Vance Products, Inc.
Vance Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1982.
Top product codes for Vance Products, Inc.
Recent clearances by Vance Products, Inc.
- K812995 — VANCE-JACOBELLIS MICROHEMATURIA CATHETER
- K820313 — VPI-FAIR URETHRAL STENT
- K813278 — VPI URETERAL DILATATION BALLON CATHETER
- K812785 — VANCE-AMBROSE RESECTOSCOPE FORCEPS
- K812057 — VANCE CYSTOSCOPIC
- K811833 — VNACE FASCIAL DILATOR SET
- K811454 — VANCE PROSTATIC ASPIRATION SET
- K810367 — KISH URETHRAL ILLUMINATED CATHETER SET
- K810368 — VANCE PERCUTANEOUS MALECOT NEPHROSTOMY
- K810370 — POLLACK CHAIN CYSOURETHROGRAM SET
- K810371 — VANCE URETHAL DILATOR SET
- K810372 — VANCE DEFLECTABLE BIOPSY BRUSH SET
- K803048 — VANCE UROSTOMY APPLIANCE
- K792219 — VANCE MALLEABLE TIP FILIFORM
- K792220 — VANCE KIDNEY BIOPSY BRUSHES
- K792221 — VANCE PHILIPS FOLLOWER CATHETER & BOUGIE
- K780765 — PERCUTANEOUS SURAPUBIC CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.