Airos Medical Inc
United StatesFDA applicant, unverified FDA FEI 3014491159
- Devices
- 109
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 109 devicesDeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
AIROS 6 Sequential Compression Device Ref K172770
Regimes: 510(k) Registry: 510(k)AIROS 8 Sequential Compression Device Ref K193068
Regimes: 510(k) Registry: 510(k)AIROS 8P Sequential Compression Device Ref K223193
Regimes: 510(k) Registry: 510(k)AIROS 6P Sequential Compression Device Ref K223195
Regimes: 510(k) Registry: 510(k)ARTAIRA Arterial Compression Device (AACD01) Ref K240499
Regimes: 510(k) Registry: 510(k)AIROS 6 Sequential Compression Device Ref K193069
Regimes: 510(k) Registry: 510(k)AIROS 8 Sequential Compression Device Ref K172779
Regimes: 510(k) Registry: 510(k)
Showing 101-109 of 109
Company details
- FDA FEI number
- 3014491159
- DUNS number
- 080942280
- Address
- 2501 MONROE BLVD STE 1200, Audubon, PA, 19403
- [email protected]
- Phone
- +1(866)991-6956