Amrex-Zetron, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2011115
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hydropulse(Grossan);inflat Tube Mass Ref K834507
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2011115
- Address
- 7034 Jackson St, Paramount, CA, 90723
Frequently asked questions
How many devices does AMREX-ZETRON, INC. have in the registry?
The registry currently lists 1 device for AMREX-ZETRON, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list AMREX-ZETRON, INC.'s devices?
Among its 1 most recently registered device, AMREX-ZETRON, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do AMREX-ZETRON, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for AMREX-ZETRON, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AMREX-ZETRON, INC. in the registry?
The most recently registered devices listed for AMREX-ZETRON, INC. include HYDROPULSE(GROSSAN);INFLAT TUBE MASS.