Beech Medical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Beech Pro Lok Fixed Ref K946082
Regimes: 510(k) Registry: 510(k)Beech Versa Lok Ref K933749
Regimes: 510(k) Registry: 510(k)Pro-Lok Extension Set Ref K933852
Regimes: 510(k) Registry: 510(k)Selfshield Hn Self Sheathing Hypodermic Needle Ref K972469
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Beech Medical Products, Inc. have in the registry?
The registry currently lists 4 devices for Beech Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beech Medical Products, Inc.'s devices?
Among its 4 most recently registered devices, Beech Medical Products, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Beech Medical Products, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Beech Medical Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beech Medical Products, Inc. in the registry?
The most recently registered devices listed for Beech Medical Products, Inc. include BEECH PRO LOK FIXED, BEECH VERSA LOK, PRO-LOK EXTENSION SET and SELFSHIELD HN SELF SHEATHING HYPODERMIC NEEDLE.