Atmos Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3005527904
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Atmos S041 Wound Ref K090130
Regimes: 510(k) Registry: 510(k)Atmos E 201 Thorax And Atmos S 201 Thorax Ref K103042
Regimes: 510(k) Registry: 510(k)Atmos C361/C451 Suction Pump Ref K090445
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3005527904
- Address
- 29 Dowlin Forge Road, Exton, PA, 19341
Frequently asked questions
How many devices does ATMOS INC. have in the registry?
The registry currently lists 3 devices for ATMOS INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ATMOS INC.'s devices?
Among its 3 most recently registered devices, ATMOS INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do ATMOS INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for ATMOS INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ATMOS INC. in the registry?
The most recently registered devices listed for ATMOS INC. include ATMOS S041 WOUND, ATMOS E 201 THORAX AND ATMOS S 201 THORAX and ATMOS C361/C451 SUCTION PUMP.