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Vance Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K812995VANCE-JACOBELLIS MICROHEMATURIA CATHETERMarch 1, 1982
K820313VPI-FAIR URETHRAL STENTMarch 1, 1982
K813278VPI URETERAL DILATATION BALLON CATHETERDecember 18, 1981
K812785VANCE-AMBROSE RESECTOSCOPE FORCEPSNovember 16, 1981
K812057VANCE CYSTOSCOPICJuly 31, 1981
K811833VNACE FASCIAL DILATOR SETJuly 10, 1981
K811454VANCE PROSTATIC ASPIRATION SETJune 9, 1981
K810372VANCE DEFLECTABLE BIOPSY BRUSH SETMarch 20, 1981
K810367KISH URETHRAL ILLUMINATED CATHETER SETMarch 20, 1981
K810368VANCE PERCUTANEOUS MALECOT NEPHROSTOMYMarch 20, 1981
K810370POLLACK CHAIN CYSOURETHROGRAM SETMarch 20, 1981
K810371VANCE URETHAL DILATOR SETMarch 20, 1981
K803048VANCE UROSTOMY APPLIANCEDecember 22, 1980
K792219VANCE MALLEABLE TIP FILIFORMDecember 6, 1979
K792220VANCE KIDNEY BIOPSY BRUSHESDecember 6, 1979
K792221VANCE PHILIPS FOLLOWER CATHETER & BOUGIEDecember 6, 1979
K780765PERCUTANEOUS SURAPUBIC CATHETERJuly 17, 1978