Surgitek - FDA 510(k) Cleared Devices
29
Total
28
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgitek Gastroenterology & Urology ✕
23 devices
Cleared
Mar 06, 1995
QUADRA-COIL URETERAL STENT
Gastroenterology & Urology
69d
Cleared
Feb 07, 1995
OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM
Gastroenterology & Urology
151d
Cleared
May 24, 1994
SURGITEK INFUSER
Gastroenterology & Urology
32d
Cleared
Jan 11, 1994
HELICAL STONE/FLATWIRE STONE BASKETS
Gastroenterology & Urology
189d
Cleared
Jan 11, 1994
GRASPING FORCEPS
Gastroenterology & Urology
189d
Cleared
Jul 23, 1993
URETERAL STENT
Gastroenterology & Urology
162d
Cleared
Jul 16, 1993
URETERAL CATHETER
Gastroenterology & Urology
168d
Cleared
Mar 05, 1993
HYDROPHILIC COATED GUIDEWIRE
Gastroenterology & Urology
78d
Cleared
Sep 17, 1992
ENDOTEK ULTRA SYSTEM
Gastroenterology & Urology
226d
Cleared
Aug 19, 1992
GRASPING FORCEPS
Gastroenterology & Urology
82d
Cleared
Mar 05, 1991
SURGITEK GRADUATED URETEROSCOPE (MODEL GU-8)
Gastroenterology & Urology
133d
Cleared
Mar 05, 1991
SURGITEK GRADUATED CYSTOSCOPE (MODEL GC-16)
Gastroenterology & Urology
133d