Medical Device Consultants, Inc.
Medical Device Consultants, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 2002.
Top product codes for Medical Device Consultants, Inc.
Recent clearances by Medical Device Consultants, Inc.
- K022895 — ELCAM STOPCOCKS AND MANIFOLDS
- K002699 — PARIETEX COMPOSITE (PCO) MESH
- K002116 — S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0
- K000551 — IMAGE X-70 PLUS DENTAL X-RAY UNIT
- K974164 — SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE
- K864282 — GLUCOSE TESTCARD USE W/ILEX PROMPT CLINICAL CH ANA
- K860122 — HEMOTEC ACT HIGH RANGE ACTIVATED CLOTTING TIME
- K860929 — ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT
- K860930 — ULTRASUN 2500 SUNTANNING UNIT
- K860931 — ULTRASUN 3000 AND 5000 SUNTANNING UNIT
- K860932 — ULTRASUN 1000 & 2000 SUNTANNING UNIT
- K853198 — ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES
- K840449 — AMICON DIAFILTER 40. HEMOFILTER
- K821651 — E-Z UP ARTHERAPEDIC CHAIR
Data sourced from openFDA. This site is unofficial and independent of the FDA.