Medical Device Consultants, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Medical Device Consultants, Inc. has 14 FDA 510(k) cleared medical devices. Based in N. Attleboro, US.
Historical record: 14 cleared submissions from 1982 to 2002.
Browse the FDA 510(k) cleared devices submitted by Medical Device Consultants, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Oct 18, 2002
ELCAM STOPCOCKS AND MANIFOLDS
General Hospital
45d
Cleared
Feb 15, 2001
PARIETEX COMPOSITE (PCO) MESH
General & Plastic Surgery
169d
Cleared
Aug 09, 2000
S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0
Cardiovascular
27d
Cleared
Mar 16, 2000
IMAGE X-70 PLUS DENTAL X-RAY UNIT
Radiology
27d
Cleared
Dec 18, 1997
SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE
Gastroenterology & Urology
43d
Cleared
May 26, 1987
GLUCOSE TESTCARD USE W/ILEX PROMPT CLINICAL CH ANA
Chemistry
208d
Cleared
Apr 04, 1986
HEMOTEC ACT HIGH RANGE ACTIVATED CLOTTING TIME
Hematology
80d
Cleared
Mar 28, 1986
ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT
General & Plastic Surgery
17d
Cleared
Mar 28, 1986
ULTRASUN 2500 SUNTANNING UNIT
General & Plastic Surgery
17d
Cleared
Mar 28, 1986
ULTRASUN 3000 AND 5000 SUNTANNING UNIT
General & Plastic Surgery
17d
Cleared
Mar 28, 1986
ULTRASUN 1000 & 2000 SUNTANNING UNIT
General & Plastic Surgery
17d
Cleared
Oct 04, 1985
ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES
Hematology
66d
Cleared
Mar 23, 1984
AMICON DIAFILTER 40. HEMOFILTER
Gastroenterology & Urology
51d
Cleared
Jun 24, 1982
E-Z UP ARTHERAPEDIC CHAIR
Physical Medicine
20d