Dws, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
Catalogue
Bi-Flow Needle Ref K761051
510(k) 510(k)Heparin Pump Ref K761050
510(k) 510(k)
Frequently asked questions
How many devices does Dws, Inc. have in the registry?
The registry currently lists 2 devices for Dws, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dws, Inc.'s devices?
Among its 2 most recently registered devices, Dws, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dws, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dws, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dws, Inc. in the registry?
The most recently registered devices listed for Dws, Inc. include BI-FLOW NEEDLE and HEPARIN PUMP.