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Difference between revisions of "Synapse Biomedical"
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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=pma&id=P200018 P200018] || Diaphragmatic/Phrenic Nerve Laparoscopically-Implanted Stimulator || f || Anesthesiology || True || False | + | | [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P200018 P200018] || Diaphragmatic/Phrenic Nerve Laparoscopically-Implanted Stimulator || f || Anesthesiology || True || False |
|} | |} | ||
+ | |||
+ | ==Hardware== | ||
+ | *[[BrainScope|BrainScope]] | ||
==Links== | ==Links== | ||
Latest revision as of 22:58, 17 February 2024
"Synapse Biomedical Inc (SBI) was founded in September 2002 to commercialize the NeuRx Diaphragm Pacing System (DPS)r that has been developed over a twenty-year period at Case Western Reserve University and the University Hospitals of Cleveland. The innovative research performed at these institutions has led to significant advances in the state of the art of electrical stimulation for the treatment of chronic respiratory insufficiency."
Founded in The United States around 2002, Synapse Biomedical produces invasive hardware.
Synapse Biomedical makes tools for medical diagnosis and treatment through body/mind state interpretation and/or neurostimulation therapies.
BCI Categories: Open-Loop Afferent
Neurostimulation Technique(s): PNS
FDA
Synapse Biomedical has 1 medical devices registered with the FDA. Here are some of them:
Device ID | Device Name | Class | Category | PMA | PMN |
---|---|---|---|---|---|
P200018 | Diaphragmatic/Phrenic Nerve Laparoscopically-Implanted Stimulator | f | Anesthesiology | True | False |