Cyberkinetics Neurotechnology Systems, Inc.
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Neuroport Electrode Ref K070272
510(k) 510(k)
FDA recalls
2009
- 4 Feb 2009 Z-1553-2009 Unclassified (pre-2012) Terminated Sterility of product cannot be assured
Frequently asked questions
How many devices does Cyberkinetics Neurotechnology Systems, Inc. have in the registry?
The registry currently lists 1 device for Cyberkinetics Neurotechnology Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cyberkinetics Neurotechnology Systems, Inc.'s devices?
Among its 1 most recently registered device, Cyberkinetics Neurotechnology Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cyberkinetics Neurotechnology Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cyberkinetics Neurotechnology Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Cyberkinetics Neurotechnology Systems, Inc.?
FDA recall records list 1 recall initiated by Cyberkinetics Neurotechnology Systems, Inc., the most recent initiated on 2009-02-04. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Cyberkinetics Neurotechnology Systems, Inc. in the registry?
The most recently registered devices listed for Cyberkinetics Neurotechnology Systems, Inc. include NEUROPORT ELECTRODE.