D.R.O. Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Flow Med 160 Ref K801004
Regimes: 510(k) Registry: 510(k)Flow Med 311 Ref K820165
Regimes: 510(k) Registry: 510(k)Flow Med Sk 140 Buret Ref K844820
Regimes: 510(k) Registry: 510(k)Flow Med 150 Ref K801821
Regimes: 510(k) Registry: 510(k)Flow Med 160 Ref K801179
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does D.R.O. Medical, Inc. have in the registry?
The registry currently lists 5 devices for D.R.O. Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D.R.O. Medical, Inc.'s devices?
Among its 5 most recently registered devices, D.R.O. Medical, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do D.R.O. Medical, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for D.R.O. Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D.R.O. Medical, Inc. in the registry?
The most recently registered devices listed for D.R.O. Medical, Inc. include FLOW MED 160, FLOW MED 311, FLOW MED SK 140 BURET and FLOW MED 150.