Intl. Cytobrush, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Intl. Cytobrush, Inc. makes
Intl. Cytobrush, Inc. manufactures cytology collection devices including the Endobrush(TM) device, Omnibbrush, Pap smear kits, Pap smear trays, and Chlamydia and STD kits for specimen collection in gynecological and diagnostic procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Endobrush(Tm) Device; Omnibrush Ref K897070
Regimes: 510(k) Registry: 510(k)Chlamydia Kit, Std Kit Ref K862322
Regimes: 510(k) Registry: 510(k)Pap Smear Kit Ref K861389
Regimes: 510(k) Registry: 510(k)Pap Smear Tray Ref K895675
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intl. Cytobrush, Inc. have in the registry?
The registry currently lists 4 devices for Intl. Cytobrush, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intl. Cytobrush, Inc.'s devices?
Among its 4 most recently registered devices, Intl. Cytobrush, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Intl. Cytobrush, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Intl. Cytobrush, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intl. Cytobrush, Inc. in the registry?
The most recently registered devices listed for Intl. Cytobrush, Inc. include ENDOBRUSH(TM) DEVICE; OMNIBRUSH, CHLAMYDIA KIT, STD KIT, PAP SMEAR KIT and PAP SMEAR TRAY.