Artemis Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Artemis Medical, Inc. makes
Artemis Medical, Inc. manufactures biopsy instruments and accessories, including the CARIS MINITOME for tissue acquisition, the 14G CORMARK Biopsy Site Identifier for marking biopsy locations, and the CARIS Site Marker for post-procedure identification.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
Caris Minitome Biopsy Instrument Ref K020024
Regimes: 510(k) Registry: 510(k)14g Cormark Biopsy Site Identifier Ref K032217
Regimes: 510(k) Registry: 510(k)Caris Site Marker Ref K003777
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artemis Medical, Inc. have in the registry?
The registry currently lists 3 devices for Artemis Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artemis Medical, Inc.'s devices?
Among its 3 most recently registered devices, Artemis Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Artemis Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Artemis Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artemis Medical, Inc. in the registry?
The most recently registered devices listed for Artemis Medical, Inc. include CARIS MINITOME BIOPSY INSTRUMENT, 14G CORMARK BIOPSY SITE IDENTIFIER and CARIS SITE MARKER.