Occumedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Occumedics, Inc. makes
Occumedics, Inc. manufactures sterile, single-use medical packaging solutions, including the OCCUPAK and ULTRAPAK systems designed for protective containment of medical devices and supplies.
These products are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Occupak CAT.#200-0538 Ref K802691
Regimes: 510(k) Registry: 510(k)Ultrapak Cat. #100-0251 Ref K802690
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Occumedics, Inc. have in the registry?
The registry currently lists 2 devices for Occumedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Occumedics, Inc.'s devices?
Among its 2 most recently registered devices, Occumedics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Occumedics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Occumedics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Occumedics, Inc. in the registry?
The most recently registered devices listed for Occumedics, Inc. include OCCUPAK CAT.#200-0538 and ULTRAPAK CAT. #100-0251.