Vance Products, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vance Products, Inc. Gastroenterology & Urology ✕
16 devices
Cleared
Mar 01, 1982
VANCE-JACOBELLIS MICROHEMATURIA CATHETER
Gastroenterology & Urology
126d
Cleared
Mar 01, 1982
VPI-FAIR URETHRAL STENT
Gastroenterology & Urology
24d
Cleared
Dec 18, 1981
VPI URETERAL DILATATION BALLON CATHETER
Gastroenterology & Urology
25d
Cleared
Jul 31, 1981
VANCE CYSTOSCOPIC
Gastroenterology & Urology
10d
Cleared
Jul 10, 1981
VNACE FASCIAL DILATOR SET
Gastroenterology & Urology
10d
Cleared
Jun 09, 1981
VANCE PROSTATIC ASPIRATION SET
Gastroenterology & Urology
18d
Cleared
Mar 20, 1981
KISH URETHRAL ILLUMINATED CATHETER SET
Gastroenterology & Urology
36d
Cleared
Mar 20, 1981
VANCE PERCUTANEOUS MALECOT NEPHROSTOMY
Gastroenterology & Urology
36d
Cleared
Mar 20, 1981
POLLACK CHAIN CYSOURETHROGRAM SET
Gastroenterology & Urology
36d
Cleared
Mar 20, 1981
VANCE URETHAL DILATOR SET
Gastroenterology & Urology
36d
Cleared
Mar 20, 1981
VANCE DEFLECTABLE BIOPSY BRUSH SET
Gastroenterology & Urology
36d
Cleared
Dec 22, 1980
VANCE UROSTOMY APPLIANCE
Gastroenterology & Urology
21d