Altaire Pharmaceuticals, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000119582
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Altaire MPS#1 Multipurpose Contact Lens Solution Ref K062332
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000119582
- Address
- 311 WEST LN., AQUEBOGUE, NY, 11931
Frequently asked questions
How many devices does ALTAIRE PHARMACEUTICALS, INC. have in the registry?
The registry currently lists 1 device for ALTAIRE PHARMACEUTICALS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ALTAIRE PHARMACEUTICALS, INC.'s devices?
Among its 1 most recently registered device, ALTAIRE PHARMACEUTICALS, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do ALTAIRE PHARMACEUTICALS, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for ALTAIRE PHARMACEUTICALS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ALTAIRE PHARMACEUTICALS, INC. in the registry?
The most recently registered devices listed for ALTAIRE PHARMACEUTICALS, INC. include ALTAIRE MPS#1 MULTIPURPOSE CONTACT LENS SOLUTION.