Contraves Medical Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Digicell 300 System Ref K873271
Regimes: 510(k) Registry: 510(k)Autolyzer 801 System (Automated Cell Counter) Ref K875346
Regimes: 510(k) Registry: 510(k)Digicell 500 Ref K873252
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Contraves Medical Instruments, Inc. have in the registry?
The registry currently lists 3 devices for Contraves Medical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Contraves Medical Instruments, Inc.'s devices?
Among its 3 most recently registered devices, Contraves Medical Instruments, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Contraves Medical Instruments, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Contraves Medical Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Contraves Medical Instruments, Inc. in the registry?
The most recently registered devices listed for Contraves Medical Instruments, Inc. include DIGICELL 300 SYSTEM, AUTOLYZER 801 SYSTEM (AUTOMATED CELL COUNTER) and DIGICELL 500.