Gaymar Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gaymar Industries, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Gaymar Industries, Inc. has 27 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 27 cleared submissions from 1976 to 2011. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Gaymar Industries, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gaymar Industries, Inc.
27 devices
Cleared
Jan 20, 2011
MEDI-THERM HYPER/HYPOTHERMIA SYSTEM, MODELS MTA6900, MTA7900
Cardiovascular
324d
Cleared
May 08, 2008
T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP
Physical Medicine
132d
Cleared
Apr 30, 1997
CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEM
Physical Medicine
287d
Cleared
Jan 28, 1997
SOF. PRESS EPC 51 SYSTEM
Cardiovascular
174d
Cleared
Aug 09, 1996
SPR PLUS II OVERLAY SYSTEM (CL250/CL212
General Hospital
87d
Cleared
May 23, 1995
TC 3000
Cardiovascular
340d
Cleared
Aug 06, 1993
TC2000 POWER UNIT AND ACCESSORIES
Cardiovascular
193d
Cleared
Mar 12, 1992
SCM-3 AND ACCESSORIES
General Hospital
129d
Cleared
Jan 07, 1992
TC-1000, TC-1050 SYSTEM
Cardiovascular
75d
Cleared
Nov 13, 1991
CLA-1400 SYSTEM
Physical Medicine
16d
Cleared
Jul 30, 1991
MEDI-THERM (MTA-5900) & DETACHABLE HOSES
Cardiovascular
82d
Cleared
Jul 13, 1988
CLINI-CARE + PRESSURE ULCER TREATMENT SYSTEM
General Hospital
55d