Medical Device Manufacturer · US , San Diego , CA

Medart Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1999

Total

Cleared

Denied

Medart Corp. has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 5 cleared submissions from 1999 to 2001. Primary specialty: General & Plastic Surgery.

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

Medart 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 - Medart Corp.

5 devices

1-5 of 5