Biocor Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Biocor Medical, Inc. makes
Biocor Medical, Inc. manufactures sterile surgical drapes and angiography drape packs designed for use in medical procedures to maintain a clean field and prevent contamination.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Surgical Drape Ref K910084
Regimes: 510(k) Registry: 510(k)Angiography Drape Pack Ref K902293
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biocor Medical, Inc. have in the registry?
The registry currently lists 2 devices for Biocor Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biocor Medical, Inc.'s devices?
Among its 2 most recently registered devices, Biocor Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biocor Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biocor Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biocor Medical, Inc. in the registry?
The most recently registered devices listed for Biocor Medical, Inc. include SURGICAL DRAPE and ANGIOGRAPHY DRAPE PACK.