Neurorecovery, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Neurorecovery, Inc. makes
Neurorecovery, Inc. manufactures medical devices for intracranial pressure monitoring and management, including a comprehensive evaluation and relief kit and a ventricular catheter with main valve assembly.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Neurorecovery, Inc. (Nri) Comprehensive Intracranial Pressure Evaluation And Relief (Ciper) Kit Ref K051599
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurorecovery, Inc. have in the registry?
The registry currently lists 2 devices for Neurorecovery, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurorecovery, Inc.'s devices?
Among its 2 most recently registered devices, Neurorecovery, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neurorecovery, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neurorecovery, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurorecovery, Inc. in the registry?
The most recently registered devices listed for Neurorecovery, Inc. include NEURORECOVERY, INC. (NRI) COMPREHENSIVE INTRACRANIAL PRESSURE EVALUATION AND RELIEF (CIPER) KIT and NEURORECOVERY VENTRICULAR CATHETER & MAIN VALVE ASSEMBLY KIT.