Medical Device Manufacturer · US , Hollywood , FL

Intl. Cytobrush, Inc.

4 submissions · 4 cleared · Since 1986

Total

Cleared

Denied

Intl. Cytobrush, Inc. has 4 FDA 510(k) cleared medical devices. Based in Hollywood, US.

Historical record: 4 cleared submissions from 1986 to 1990. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Intl. Cytobrush, Inc. Filter by specialty or product code using the sidebar.

4 devices

1–4 of 4

Data Source

FDA 510(k) public files . 174,402 total devices indexed.