Vance Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vance Products, Inc. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Vance Products, Inc. has 17 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 17 cleared submissions from 1978 to 1982.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vance Products, Inc.
17 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
Nov 16, 1981
VANCE-AMBROSE RESECTOSCOPE FORCEPS
General & Plastic Surgery
42d
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