Perfusion Partners & Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Perfusion Partners & Assoc., Inc. makes
Perfusion Partners & Assoc., Inc. makes the GENESISCS Component Concentrating System and the SECQUIRE Cell Separator.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Genesiscs Component Concentrating System Ref K070666
Regimes: 510(k) Registry: 510(k)Secquire Cell Separator Ref K024080
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Perfusion Partners & Assoc., Inc. have in the registry?
The registry currently lists 2 devices for Perfusion Partners & Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Perfusion Partners & Assoc., Inc.'s devices?
Among its 2 most recently registered devices, Perfusion Partners & Assoc., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Perfusion Partners & Assoc., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Perfusion Partners & Assoc., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Perfusion Partners & Assoc., Inc. in the registry?
The most recently registered devices listed for Perfusion Partners & Assoc., Inc. include GENESISCS COMPONENT CONCENTRATING SYSTEM and SECQUIRE CELL SEPARATOR.