Medical Device Manufacturer · BR , British Isles

Bodystat , Ltd. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1995

8

Total

8

Cleared

0

Denied

Bodystat , Ltd. has 8 FDA 510(k) cleared medical devices. Based in British Isles, BR.

Historical record: 8 cleared submissions from 1995 to 2011. Primary specialty: Gastroenterology & Urology.

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

Bodystat , Ltd. is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Bodystat , Ltd.

8 devices

1-8 of 8

Cleared Feb 07, 2011

MODIFICATION TO BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT

Gastroenterology & Urology · 913d

Cleared Feb 07, 2011

QUADSCAN 4000 BODY BODY COMPOSITION, FLUID & ILLNESS/SEGMENTAL MONITORING UNIT

Gastroenterology & Urology · 913d

Cleared Nov 25, 2008

BODYSTAT 1500 BODY COMPOSITION MONITORING UNIT

Gastroenterology & Urology · 109d

Cleared Jul 03, 2001

Gastroenterology & Urology · 294d

Cleared Mar 15, 2000

BODYSTAT 1500MDD BODY COMPOSITION MONITORING UNIT

Gastroenterology & Urology · 90d

Cleared Jun 11, 1998

BODYSTAT DUALSCAN 2005

Gastroenterology & Urology · 87d

Cleared Nov 26, 1997

Gastroenterology & Urology · 210d

Cleared Nov 22, 1995

Cardiovascular · 259d