Gaymar Industries, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K100585MEDI-THERM HYPER/HYPOTHERMIA SYSTEM, MODELS MTA6900, MTA7900January 20, 2011
K073675T-PUMP LOCALIZED TEMPERATURE THERAPY PUMPMay 8, 2008
K962788CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEMApril 30, 1997
K963067SOF. PRESS EPC 51 SYSTEMJanuary 28, 1997
K961854SPR PLUS II OVERLAY SYSTEM (CL250/CL212August 9, 1996
K942881TC 3000May 23, 1995
K930345TC2000 POWER UNIT AND ACCESSORIESAugust 6, 1993
K914921SCM-3 AND ACCESSORIESMarch 12, 1992
K914805TC-1000, TC-1050 SYSTEMJanuary 7, 1992
K914851CLA-1400 SYSTEMNovember 13, 1991
K912051MEDI-THERM (MTA-5900) & DETACHABLE HOSESJuly 30, 1991
K882092CLINI-CARE + PRESSURE ULCER TREATMENT SYSTEMJuly 13, 1988
K882012LIFESTYLE SOF. CARE GEL CHAIR CUSHIONMay 23, 1988
K852943NEO SHIELDNovember 8, 1985
K851027SOF. CARE CUSHION & SOF-CARE CUSHION COVERJune 18, 1985
K832819MUL-T-PADSeptember 26, 1983
K832820MUL-T-BLANKETSeptember 26, 1983
K810543NEO-WAVE SYSTEMMarch 6, 1981
K800812MEDI-THERMApril 24, 1980
K780906AIR-FLO ALTERNATING PRESSURE PAD SYSTEMAugust 10, 1978