Stanford Scientific, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Stanford Scientific, Inc. makes
Stanford Scientific, Inc. manufactures respiratory exercise devices, including the AEROBITRON II, CHRONAEROBIC (CA-1), AEROBITRON 1, and AEROBITRON III. These products are designed for pulmonary rehabilitation and aerobic training, providing controlled resistance for respiratory muscle conditioning.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is registered in the FDA’s 510(k) database. Stanford Scientific, Inc. is based in the United States.
Catalogue
Aerobitron Ii Ref K792120
Regimes: 510(k) Registry: 510(k)Chronaerobic (Ca-1) Ref K792122
Regimes: 510(k) Registry: 510(k)Aerobitron 1 Ref K791966
Regimes: 510(k) Registry: 510(k)Aerobitron Iii Ref K792121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stanford Scientific, Inc. have in the registry?
The registry currently lists 4 devices for Stanford Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stanford Scientific, Inc.'s devices?
Among its 4 most recently registered devices, Stanford Scientific, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Stanford Scientific, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Stanford Scientific, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stanford Scientific, Inc. in the registry?
The most recently registered devices listed for Stanford Scientific, Inc. include AEROBITRON II, CHRONAEROBIC (CA-1), AEROBITRON 1 and AEROBITRON III.