Richmond Diagnostics, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3000206772
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Hematachek Ref K964452
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3000206772
- Address
- 525 Milltown Road, North Brunswick, NJ, 08902
Frequently asked questions
How many devices does RICHMOND DIAGNOSTICS, INC. have in the registry?
The registry currently lists 1 device for RICHMOND DIAGNOSTICS, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list RICHMOND DIAGNOSTICS, INC.'s devices?
Among its 1 most recently registered device, RICHMOND DIAGNOSTICS, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do RICHMOND DIAGNOSTICS, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for RICHMOND DIAGNOSTICS, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from RICHMOND DIAGNOSTICS, INC. in the registry?
The most recently registered devices listed for RICHMOND DIAGNOSTICS, INC. include HEMATACHEK.