SW Technologies Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2939388
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2939388
- Address
- 33278 CENTRAL AVE.,, UNION CITY, CA, 94587
Frequently asked questions
How many devices does SW Technologies Inc. have in the registry?
The registry currently lists 1 device for SW Technologies Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SW Technologies Inc.'s devices?
Among its 1 most recently registered device, SW Technologies Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do SW Technologies Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for SW Technologies Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SW Technologies Inc. in the registry?
The most recently registered devices listed for SW Technologies Inc. include Biodegradable Powder Free Nitrile Examination Glove, Blue Color, Tested for use with Chemotherapy drugs, Fentanyl Citrate, Simulated Gastric Acid and Fentanyl Citrate-Simulated Gastric Acid Solution.