Procedure Pak, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Procedure Pak, Inc. makes
Procedure Pak, Inc. manufactures non-sterile and sterile disposable surgical drapes, as well as surgical packs, surgical kits, and surgical trays.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Procedure Pak, Inc. is based in the US.
Catalogue
Non-Sterile & Sterile Disposable Surgical Drapes Ref K861288
Regimes: 510(k) Registry: 510(k)Surgical Packs, Surgical Kits And Surgical Trays Ref K871478
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Procedure Pak, Inc. have in the registry?
The registry currently lists 2 devices for Procedure Pak, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Procedure Pak, Inc.'s devices?
Among its 2 most recently registered devices, Procedure Pak, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Procedure Pak, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Procedure Pak, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Procedure Pak, Inc. in the registry?
The most recently registered devices listed for Procedure Pak, Inc. include NON-STERILE & STERILE DISPOSABLE SURGICAL DRAPES and SURGICAL PACKS, SURGICAL KITS AND SURGICAL TRAYS.