Western M/D, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Nutip (Tm) Syringe Shield Ref K911214
Regimes: 510(k) Registry: 510(k)Suretip Syringe Tip Cover Ref K931772
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Western M/D, Inc. have in the registry?
The registry currently lists 2 devices for Western M/D, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Western M/D, Inc.'s devices?
Among its 2 most recently registered devices, Western M/D, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Western M/D, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Western M/D, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Western M/D, Inc. in the registry?
The most recently registered devices listed for Western M/D, Inc. include NUTIP (TM) SYRINGE SHIELD and SURETIP SYRINGE TIP COVER.