Amici, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
What Amici, Inc. makes
Amici, Inc. makes respiratory therapy devices including xenon and krypton administration systems, aerosol delivery systems, nebulizers, and mouthpieces such as the Tru-Fit soft plastic mouthpiece.
The company's devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; Amici, Inc. is based in the United States.
Catalogue
Amici Xenon Rebreathing System* Ref K865084
Regimes: 510(k) Registry: 510(k)The Swirler Nebulizer Ref K952910
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Aerosol System Ref K063716
Regimes: 510(k) Registry: 510(k)Amici Krypton Administration System* Ref K872920
Regimes: 510(k) Registry: 510(k)The Swirler Aerosol System Ref K952893
Regimes: 510(k) Registry: 510(k)Amici Tru-Fit Soft Plastic Mouthpiece Ref K903694
Regimes: 510(k) Registry: 510(k)Amici Xenon Administration Set Ref K903805
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amici, Inc. have in the registry?
The registry currently lists 8 devices for Amici, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amici, Inc.'s devices?
Among its 8 most recently registered devices, Amici, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Amici, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Amici, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amici, Inc. in the registry?
The most recently registered devices listed for Amici, Inc. include AMICI XENON REBREATHING SYSTEM*, THE SWIRLER NEBULIZER, AMICI KRYPTON ADMINISTRATION SYSTEM, MODIFICATION and AEROSOL SYSTEM.