Biodynamics Corp. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Biodynamics Corp. has 21 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 21 cleared submissions from 1980 to 2006.
Browse the FDA 510(k) cleared devices submitted by Biodynamics Corp. Filter by specialty or product code using the sidebar.
21 devices
Cleared
Mar 16, 2006
BIODYNAMICS BIA 500 BIOMPEDANCE BODY COMPOSITION ANALYZER
Gastroenterology & Urology
266d
Cleared
Nov 17, 1988
BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZER
Cardiovascular
55d
Cleared
Sep 09, 1988
BIODYNAMICS AUTOTRANSFUSION RESERVOIR
Anesthesiology
148d
Cleared
Jul 28, 1988
BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER
Cardiovascular
78d
Cleared
Mar 16, 1988
BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER
Cardiovascular
145d
Cleared
Mar 09, 1988
AUTOTRANSFUSION APPARATUS
Anesthesiology
173d
Cleared
Oct 23, 1987
ADR-22 AUTOMATIC DIALYZER REPROCESSOR
Gastroenterology & Urology
18d
Cleared
Feb 27, 1987
INFUMIX MIXING CONTAINER
General Hospital
51d
Cleared
Sep 30, 1982
PLATELET CENTRIFUGE
Hematology
23d
Cleared
Sep 30, 1982
UNIVERSAL CENTRIFUGE
Hematology
23d
Cleared
Sep 02, 1982
BASIC CENTRIFUGE
Hematology
21d
Cleared
Jul 02, 1982
URICACID
Chemistry
18d