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Difference between revisions of "Incereb"
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! Device ID !! Device Name !! Class !! Category !! PMA !! PMN | ! Device ID !! Device Name !! Class !! Category !! PMA !! PMN | ||
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− | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K151576 K151576] || Electrode, Cutaneous || 2 || Neurology || False || True | + | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K151576 K151576] || Electrode, Cutaneous || 2 || Neurology || False || True |
|} | |} | ||
+ | |||
+ | ==Hardware== | ||
+ | *[[BrainScope|BrainScope]] | ||
==Links== | ==Links== | ||
Latest revision as of 22:57, 17 February 2024
Incereb is an Irish medical device early stage company in the emerging neonatal intensive care unit (NICU) market. Founded in May 2011, Incereb is headquartered in Dublin, Ireland. The company designs and develops disposable Electroencephalography (EEG) and Cerebral Function Monitoring (CFM) products for term and preterm infants (neonates). These intuitive products are designed to be used with minimal training and will significantly reduce the time taken to set up the neonate for EEG and CFM monitoring. Their products are designed to interface with all brands of EEG and CFM recording equipment.
Incereb was aquired by Lifelines Neuro.
Founded in Ireland around 2011, Incereb produces noninvasive hardware and end-user software.
Incereb 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
FDA
Incereb has 1 medical devices registered with the FDA. Here are some of them:
Device ID | Device Name | Class | Category | PMA | PMN |
---|---|---|---|---|---|
K151576 | Electrode, Cutaneous | 2 | Neurology | False | True |