Laboratoires Perouse
FranceFDA applicant, unverified
- Devices
- 1
What Laboratoires Perouse makes
Laboratoires Perouse manufactures the POLYPERF and POLYPERF SAFE, which are medical devices used for vascular access.
These devices are classified as Class II medical products and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Polyperf / Polyperf Safe Ref K063631
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laboratoires Perouse have in the registry?
The registry currently lists 1 device for Laboratoires Perouse. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laboratoires Perouse's devices?
Among its 1 most recently registered device, Laboratoires Perouse has devices listed in FDA 510(k) (1 device).
What risk classes do Laboratoires Perouse's devices fall under?
Among its 1 most recently registered device, the classes recorded for Laboratoires Perouse's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laboratoires Perouse in the registry?
The most recently registered devices listed for Laboratoires Perouse include POLYPERF / POLYPERF SAFE.