Frisco Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Boston Syringe Ref K820294
Regimes: 510(k) Registry: 510(k)Syringe, Piston Ref K812888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Frisco Products, Inc. have in the registry?
The registry currently lists 2 devices for Frisco Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Frisco Products, Inc.'s devices?
Among its 2 most recently registered devices, Frisco Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Frisco Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Frisco Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Frisco Products, Inc. in the registry?
The most recently registered devices listed for Frisco Products, Inc. include BOSTON SYRINGE and SYRINGE, PISTON.