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Difference between revisions of "Philips"

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*[[MR_7700|MR 7700]]
 
*[[MR_7700|MR 7700]]
 
*[[Spectral_CT_7500|Spectral CT 7500]]
 
*[[Spectral_CT_7500|Spectral CT 7500]]
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==FDA==
 +
Philips has 239 medical devices registered with the FDA. Here are some of them:
 +
{| class="wikitable" style="margin:auto"
 +
|+ Examples of FDA Approved Devices ([[Philips_FDA_Devices | View List]])
 +
|-
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! Device ID !! Device Name !! Class !! Category !! PMA !! PMN
 +
|-
 +
| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P960042 P960042] || Device, Removal, Pacemaker Electrode, Percutaneous || 3 || Cardiovascular || True || False
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|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P960042 P960042] || Device, Removal, Pacemaker Electrode, Percutaneous || 3 || Cardiovascular || True || False
 +
|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P180034 P180034] || Scaffold, Dissection Repair || 3 || Cardiovascular || True || False
 +
|-
 +
| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P960042 P960042] || Device, Removal, Pacemaker Electrode, Percutaneous || 3 || Cardiovascular || True || False
 +
|-
 +
| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P180034 P180034] || Scaffold, Dissection Repair || 3 || Cardiovascular || True || False
 +
|-
 +
| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K201012 K201012] || System, Imaging, Pulsed Doppler, Ultrasonic || 2 || Radiology || False || True
 +
|-
 +
| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K170144 K170144] || Interventional Fluoroscopic X-Ray System || 2 || Radiology || False || True
 +
|-
 +
| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K171314 K171314] || System, Image Processing, Radiological || 2 || Radiology || False || True
 +
|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K172406 K172406] || System, Tomography, Computed, Emission || 2 || Radiology || False || True
 +
|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K190913 K190913] || System, Image Processing, Radiological || 2 || Radiology || False || True
 +
|}
 
==Links==
 
==Links==
 +
 
[https://www.usa.philips.com Website]
 
[https://www.usa.philips.com Website]
 
[https://www.crunchbase.com/organization/philips-c6d9 Crunchbase]
 
[https://www.crunchbase.com/organization/philips-c6d9 Crunchbase]

Latest revision as of 02:28, 18 April 2023

"Philips is a health care company that focuses only on patients' proper recovery and diagnosis treatment."


Philips Company Profile

Founded in The Netherlands around 1891, Philips produces noninvasive hardware and end-user software.

Philips makes tools for medical diagnosis and treatment through body/mind state interpretation and/or neurostimulation therapies.

BCI Categories: Open-Loop Efferent

Neurosensing Technique(s): EEG, EMG, fNIRS, MRI

Hardware

FDA

Philips has 239 medical devices registered with the FDA. Here are some of them:

Examples of FDA Approved Devices ( View List)
Device ID Device Name Class Category PMA PMN
P960042 Device, Removal, Pacemaker Electrode, Percutaneous 3 Cardiovascular True False
P960042 Device, Removal, Pacemaker Electrode, Percutaneous 3 Cardiovascular True False
P180034 Scaffold, Dissection Repair 3 Cardiovascular True False
P960042 Device, Removal, Pacemaker Electrode, Percutaneous 3 Cardiovascular True False
P180034 Scaffold, Dissection Repair 3 Cardiovascular True False
K201012 System, Imaging, Pulsed Doppler, Ultrasonic 2 Radiology False True
K170144 Interventional Fluoroscopic X-Ray System 2 Radiology False True
K171314 System, Image Processing, Radiological 2 Radiology False True
K172406 System, Tomography, Computed, Emission 2 Radiology False True
K190913 System, Image Processing, Radiological 2 Radiology False True

Links

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