Medical Device Manufacturer · US , Skokie , IL

Tanita Corp. of America - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1993

Total

Cleared

Denied

Tanita Corp. of America has 6 FDA 510(k) cleared medical devices. Based in Skokie, US.

Historical record: 6 cleared submissions from 1993 to 2004. Primary specialty: Gastroenterology & Urology.

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

Tanita Corp. of America 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 - Tanita Corp. of America

6 devices

1-6 of 6