Medical Device Manufacturer · US , Hackensack , NJ

Xylog Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1988

Total

Cleared

Denied

Xylog Corp. has 4 FDA 510(k) cleared medical devices. Based in Hackensack, US.

Historical record: 4 cleared submissions from 1988 to 1994. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Xylog Corp. Filter by specialty or product code using the sidebar.

Xylog Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Xylog Corp.

4 devices

1-4 of 4