Biomedical Devices, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Biomedical Devices, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1983 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biomedical Devices, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Dec 26, 1995
THE REEL THING (MODIFICATION)
General & Plastic Surgery
43d
Cleared
Jun 28, 1994
BIO-PREP CEMENT RESTRICTOR
Orthopedic
441d
Cleared
Jan 21, 1994
BIO-PREP
Orthopedic
283d
Cleared
Oct 07, 1993
BMD AIR/OXYGEN BLENDER
Anesthesiology
316d
Cleared
Oct 19, 1990
STERI-SHIELD
General Hospital
74d
Cleared
Aug 17, 1990
STERI-SHIELD
General Hospital
60d
Cleared
Mar 31, 1983
PUMP PALL AMBULATORY INSULIN INFUSION
General Hospital
34d