International Regulatory Consultants - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
International Regulatory Consultants has 5 FDA 510(k) cleared medical devices. Based in Efrat, Israel, IL.
Historical record: 5 cleared submissions from 1994 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by International Regulatory Consultants Filter by specialty or product code using the sidebar.
5 devices
Cleared
Oct 09, 1998
VORTEK URETERAL DOUBLE LOOP STENT, BIOSOFT URETERAL DOUBLE LOOP STENT
Gastroenterology & Urology
158d
Cleared
Jul 03, 1997
MEDISURF
Radiology
84d
Cleared
Sep 06, 1996
SHIFA STERILE DISPOSABLE SYRINGES
General Hospital
65d
Cleared
Aug 18, 1995
DISPOMEDIC DISPOSABLE SYRINGES AND NEEDLES
General Hospital
227d
Cleared
Oct 19, 1994
MEMOTHERM 10 BABY THERMOMETER
General Hospital
350d