Biomedical Dynamics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomedical Dynamics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Biomedical Dynamics, Inc. has 10 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 10 cleared submissions from 1985 to 1992. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biomedical Dynamics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomedical Dynamics, Inc.
10 devices
Cleared
Feb 05, 1992
IRRIGATOR/ASPIRATOR PROBE
Ophthalmic
89d
Cleared
Jan 09, 1992
PRESSURE INFUSER
General Hospital
141d
Cleared
Aug 07, 1991
CUFFABLE
Cardiovascular
141d
Cleared
Jul 22, 1991
INFUSABLE
General Hospital
125d
Cleared
Jun 24, 1991
IRRIGATION/ASPIRATION TUBING SET
Gastroenterology & Urology
90d
Cleared
Dec 20, 1990
ANEROID BLOOD PRESSURE GAUGE
Gastroenterology & Urology
86d
Cleared
May 05, 1989
PRESSURE INFUSOR FOR I.V. BAGS/AUTOINFLATION
General Hospital
107d
Cleared
Oct 14, 1988
BLOOD PRESSURE CUFF
Cardiovascular
170d
Cleared
Jul 15, 1986
BIOMEDICAL DYNAMICS DISPOSABLE PRESSURE INFUSOR
General Hospital
55d
Cleared
Apr 01, 1985
CORRECT FLO INTRAVASCULAR ADMINISTRATION SET
General Hospital
52d