Intramed Laboratories, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Intramed Laboratories, Inc. has 14 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 14 cleared submissions from 1987 to 1996.
Browse the FDA 510(k) cleared devices submitted by Intramed Laboratories, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Jan 05, 1996
TITANIUM HEMOSTATIC CLIP
General & Plastic Surgery
177d
Cleared
Feb 07, 1995
GRAFT THROMBECTOMY INSTRUMENTS
Cardiovascular
259d
Cleared
Jun 13, 1994
ARTHROSCOPE
Ophthalmic
427d
Cleared
Feb 10, 1994
VALVULOTOME
Cardiovascular
478d
Cleared
Jan 18, 1994
ANGIOSCOPE
Cardiovascular
110d
Cleared
Aug 03, 1992
ENDOSCOPIC RETRIEVAL BASKET
Gastroenterology & Urology
90d
Cleared
Mar 02, 1992
OPTICAL VALVULOTOME
Cardiovascular
153d
Cleared
Dec 20, 1990
FLEXIBLE ARTHROSCOPE
Orthopedic
80d
Cleared
Sep 04, 1990
LAPAROSCOPE
Obstetrics & Gynecology
29d
Cleared
Aug 30, 1990
CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
General Hospital
90d
Cleared
May 22, 1990
FLEXIBLE CHOLEDOCHOSCOPE
Gastroenterology & Urology
78d
Cleared
Mar 07, 1990
ANGIOSCOPE
Cardiovascular
232d