Vance Products, Inc.
Vance Products, Inc. appears in FDA public data with 0 recalls, 17 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 1, 1982.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 17
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K820313 | VPI-FAIR URETHRAL STENT | March 1, 1982 |
| K812995 | VANCE-JACOBELLIS MICROHEMATURIA CATHETER | March 1, 1982 |
| K813278 | VPI URETERAL DILATATION BALLON CATHETER | December 18, 1981 |
| K812785 | VANCE-AMBROSE RESECTOSCOPE FORCEPS | November 16, 1981 |
| K812057 | VANCE CYSTOSCOPIC | July 31, 1981 |
| K811833 | VNACE FASCIAL DILATOR SET | July 10, 1981 |
| K811454 | VANCE PROSTATIC ASPIRATION SET | June 9, 1981 |
| K810367 | KISH URETHRAL ILLUMINATED CATHETER SET | March 20, 1981 |
| K810372 | VANCE DEFLECTABLE BIOPSY BRUSH SET | March 20, 1981 |
| K810370 | POLLACK CHAIN CYSOURETHROGRAM SET | March 20, 1981 |
| K810368 | VANCE PERCUTANEOUS MALECOT NEPHROSTOMY | March 20, 1981 |
| K810371 | VANCE URETHAL DILATOR SET | March 20, 1981 |
| K803048 | VANCE UROSTOMY APPLIANCE | December 22, 1980 |
| K792219 | VANCE MALLEABLE TIP FILIFORM | December 6, 1979 |
| K792220 | VANCE KIDNEY BIOPSY BRUSHES | December 6, 1979 |
| K792221 | VANCE PHILIPS FOLLOWER CATHETER & BOUGIE | December 6, 1979 |
| K780765 | PERCUTANEOUS SURAPUBIC CATHETER | July 17, 1978 |