Precision Surgical Instrument, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Microinfertility Scissors, Titanium Ref K844822
Regimes: 510(k) Registry: 510(k)Microinfertility Needle Holder, Titanium Ref K844821
Regimes: 510(k) Registry: 510(k)Microinfertility Forceps, Titanium Ref K844823
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precision Surgical Instrument, Inc. have in the registry?
The registry currently lists 3 devices for Precision Surgical Instrument, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Surgical Instrument, Inc.'s devices?
Among its 3 most recently registered devices, Precision Surgical Instrument, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Precision Surgical Instrument, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Precision Surgical Instrument, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precision Surgical Instrument, Inc. in the registry?
The most recently registered devices listed for Precision Surgical Instrument, Inc. include MICROINFERTILITY SCISSORS, TITANIUM, MICROINFERTILITY NEEDLE HOLDER, TITANIUM and MICROINFERTILITY FORCEPS, TITANIUM.