Diatron Us Inc
Country not established FDA establishment FEI 3008425728
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Abacus 5 Ref K112755
510(k) 510(k)Abacus 3CP Ref K111534
510(k) 510(k)
Company details
- FDA FEI number
- 3008425728
- Address
- 12601 NW 115th Avenue, Medley, FL, 33178
Frequently asked questions
How many devices does DIATRON US INC have in the registry?
The registry currently lists 2 devices for DIATRON US INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list DIATRON US INC's devices?
Among its 2 most recently registered devices, DIATRON US INC has devices listed in FDA 510(k) (2 devices).
What risk classes do DIATRON US INC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for DIATRON US INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from DIATRON US INC in the registry?
The most recently registered devices listed for DIATRON US INC include ABACUS 5 and ABACUS 3CP.