Vance Products, Inc.
Mchenry, IL, US
Vance Products, Inc. appears in FDA device records in Mchenry, IL. FDA records list 17 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 17
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 17 510(k) clearances for Vance Products, Inc. between 1978 and 1982. The busiest year on record is 1981, with 10. The most recent is 1982, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1979 | 3 |
| 1980 | 1 |
| 1981 | 10 |
| 1982 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K820313 | VPI-FAIR URETHRAL STENT | KOD | Substantially Equivalent | |
| K812995 | VANCE-JACOBELLIS MICROHEMATURIA CATHETER | KOD | Substantially Equivalent | |
| K813278 | VPI URETERAL DILATATION BALLON CATHETER | EZN | Substantially Equivalent | |
| K812785 | VANCE-AMBROSE RESECTOSCOPE FORCEPS | GEN | Substantially Equivalent | |
| K812057 | VANCE CYSTOSCOPIC | FBK | Substantially Equivalent | |
| K811833 | VNACE FASCIAL DILATOR SET | KOE | Substantially Equivalent | |
| K811454 | VANCE PROSTATIC ASPIRATION SET | KNW | Substantially Equivalent | |
| K810372 | VANCE DEFLECTABLE BIOPSY BRUSH SET | KOD | Substantially Equivalent | |
| K810371 | VANCE URETHAL DILATOR SET | KOE | Substantially Equivalent | |
| K810370 | POLLACK CHAIN CYSOURETHROGRAM SET | FGI | Substantially Equivalent | |
| K810368 | VANCE PERCUTANEOUS MALECOT NEPHROSTOMY | KOB | Substantially Equivalent | |
| K810367 | KISH URETHRAL ILLUMINATED CATHETER SET | KOD | Substantially Equivalent | |
| K803048 | VANCE UROSTOMY APPLIANCE | EXB | Substantially Equivalent | |
| K792221 | VANCE PHILIPS FOLLOWER CATHETER & BOUGIE | KOE | Substantially Equivalent | |
| K792220 | VANCE KIDNEY BIOPSY BRUSHES | KOD | Substantially Equivalent | |
| K792219 | VANCE MALLEABLE TIP FILIFORM | KOE | Substantially Equivalent | |
| K780765 | PERCUTANEOUS SURAPUBIC CATHETER | KOB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain