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Vas-Cath, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K973013OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETERJune 19, 1998
K965178NIAGARA DUAL LUMEN CATHETERAugust 19, 1997
K964881ULTRAVERSE PTA CATHETERMay 28, 1997
K970725OPTI-PLAST XL 5.5 F PTA CATHETERMay 9, 1997
K941706OPTI-PLAST ANGIOPLASTY CATHETEROctober 18, 1994
K925485VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETERMarch 10, 1994
K933483OPTI-PLAST 5F PTA CATHETERSSeptember 24, 1993
K914210VAS-CATH DUALATOR(TM) VESSEL DILATORJuly 1, 1993
K914162VAS-CATH FLEXXICON 2 DUAL LUMEN DIALYSIS CATHETERSJuly 1, 1993
K914976OPTI-PLAST 5F PTA CATHETERS, MODIFICATIONJanuary 27, 1992
K914500OPTI-PLAST 5F PTA CATHETERS, MODIFICATIONDecember 31, 1991
K913112OPTI-PLAST 5F PTA CATHETERSAugust 16, 1991
K912984OPTI-PLAST 5F PTA CATHETERS, MODIFICATIONAugust 13, 1991
K911639OPTI-PLAST 5F PTA CATHETERS OVEN CURING PROCEDUREJune 11, 1991
K910996OPTI-PLAST 5F PTA CATHETERSApril 9, 1991
K905505VAS-CATH URETERAL STENTS CATHETER, MODIFICATIONApril 9, 1991
K903417VAS-CATH OPTI-PLAST 5F PERIPHERAL ANGIOPLASTY CATHDecember 5, 1990
K902367OPTI-PLAST 7F PERIPHERAL ANGIOPLASTY CATHETERDecember 3, 1990
K895597VAS-CATH TRIFUSION TRIPLE LUMEN INFUSION CATHETERSeptember 12, 1990
K895506FLEXXICON PLUS DUAL LUMEN DIALYSIS CATHETERFebruary 9, 1990