Camino Neurocare, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Camino Neurocare, Inc. makes
Camino Neurocare, Inc. manufactures intracranial pressure monitoring systems, including kits for parenchymal and subdural tunneling measurements, as well as combined intracranial pressure-temperature sensing devices. These products are designed for real-time monitoring of brain pressure and temperature in clinical settings.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. Camino Neurocare, Inc. is based in the United States.
Catalogue
Parenchymal Bolt Pressure Monitoring Kit Ref K981846
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Camino Neurocare, Inc. have in the registry?
The registry currently lists 3 devices for Camino Neurocare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Camino Neurocare, Inc.'s devices?
Among its 3 most recently registered devices, Camino Neurocare, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Camino Neurocare, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Camino Neurocare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Camino Neurocare, Inc. in the registry?
The most recently registered devices listed for Camino Neurocare, Inc. include PARENCHYMAL BOLT PRESSURE MONITORING KIT, VENTRIX SUBDURAL TUNNELING PRESSURE MONITORING KIT MODEL NL950-SD and COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (ICP/).