Betaflo, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Betaflo, Inc. makes
Betaflo, Inc. manufactures the BETAFLO 2000, a medical device designed for fluid management in clinical settings, and the BETAFLO 2000 PIGGYBACK SYSTEM, an accessory for intravenous administration. These products are intended for controlled infusion and monitoring of fluids in patient care environments.
The company’s devices fall under Class II classification in the US and are listed in the FDA’s 510(k) registry. The portfolio is regulated under US medical device laws, and the manufacturer is based in the United States.
Catalogue
Betaflo 2000 Ref K862273
Regimes: 510(k) Registry: 510(k)Betaflo 2000 Piggyback System Ref K864789
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Betaflo, Inc. have in the registry?
The registry currently lists 2 devices for Betaflo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Betaflo, Inc.'s devices?
Among its 2 most recently registered devices, Betaflo, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Betaflo, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Betaflo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Betaflo, Inc. in the registry?
The most recently registered devices listed for Betaflo, Inc. include BETAFLO 2000 and BETAFLO 2000 PIGGYBACK SYSTEM.