Seabrook Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seabrook Medical Systems, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Seabrook Medical Systems, Inc. has 12 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 12 cleared submissions from 1984 to 1995. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Seabrook Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seabrook Medical Systems, Inc.
12 devices
Cleared
Sep 06, 1995
TROPICAIR CONVECTIVE WARING SYSTEM
Cardiovascular
260d
Cleared
Sep 06, 1995
TROPICAIR CONVECTIVE WARMING BLANKETS
Cardiovascular
126d
Cleared
Feb 22, 1994
COOL-AID
Physical Medicine
350d
Cleared
Jul 13, 1993
TROPIC-AIR
Cardiovascular
383d
Cleared
Oct 18, 1991
GOLDEN THERMAL(R)
Physical Medicine
30d
Cleared
Oct 22, 1990
TROPI-COOL
Cardiovascular
122d
Cleared
Jun 21, 1990
PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM.
Physical Medicine
31d
Cleared
Jun 21, 1990
ELECTRI-COOL(TM) LIQUID-CIRCULAT. THERMAL THERAPY
Physical Medicine
31d
Cleared
Sep 23, 1988
DUAL-TEMP(TM) COOLING/WARMING UNIT
Physical Medicine
112d
Cleared
Jun 22, 1988
MINI-TEMP(TM)
Cardiovascular
86d
Cleared
Dec 22, 1987
ECMO-TEMP (TM) BLOOD WARMING DEVICE
Cardiovascular
97d
Cleared
Aug 17, 1984
MICRO-TEMP PUMPS & MICRO-TEMP PADS
Physical Medicine
7d