Gaymar Industries, Inc.
Gaymar Industries, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2011.
Top product codes for Gaymar Industries, Inc.
Recent clearances by Gaymar Industries, Inc.
- K100585 — MEDI-THERM HYPER/HYPOTHERMIA SYSTEM, MODELS MTA6900, MTA7900
- K073675 — T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP
- K962788 — CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEM
- K963067 — SOF. PRESS EPC 51 SYSTEM
- K961854 — SPR PLUS II OVERLAY SYSTEM (CL250/CL212
- K942881 — TC 3000
- K930345 — TC2000 POWER UNIT AND ACCESSORIES
- K914921 — SCM-3 AND ACCESSORIES
- K914805 — TC-1000, TC-1050 SYSTEM
- K914851 — CLA-1400 SYSTEM
- K912051 — MEDI-THERM (MTA-5900) & DETACHABLE HOSES
- K882092 — CLINI-CARE + PRESSURE ULCER TREATMENT SYSTEM
- K882012 — LIFESTYLE SOF. CARE GEL CHAIR CUSHION
- K852943 — NEO SHIELD
- K851027 — SOF. CARE CUSHION & SOF-CARE CUSHION COVER
- K832819 — MUL-T-PAD
- K832820 — MUL-T-BLANKET
- K810543 — NEO-WAVE SYSTEM
- K800812 — MEDI-THERM
- K780906 — AIR-FLO ALTERNATING PRESSURE PAD SYSTEM
- K780471 — GASTRIC LAVAGE KIT
- K771083 — SEQUENTIAL PRESSURE CUFF
- K760545 — WEIGHING STATION, MOBILE PATIENT
- K760804 — T-PUMP, TEMPERATURE - THERAPY PUMP
- K760706 — MUL-T-PAD
- K760527 — T-PAD
- K760315 — PAD, POLYETHER FOAM, OPEN CELL
Data sourced from openFDA. This site is unofficial and independent of the FDA.