Gesco Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
26
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K954422PER-Q-CATH MID-LINEDecember 15, 1995
K940870UMBILI-CATHAugust 2, 1994
K940953UMBILI-CATH-SAugust 2, 1994
K940952UMBILI-CATH-S-DLJuly 29, 1994
K941672URI-CATH CATHETERMay 16, 1994
K941232THORA-CATHMay 11, 1994
K940871UMBILI-CATH-PApril 29, 1994
K931989VENTRI-CATHJuly 21, 1993
K926063PER-Q-CATH DRESSING CHANGE TRAYJune 7, 1993
K923591PALA-NATEMarch 16, 1993
K915167GESCO PER-Q-CATH CATHETER INTRODUCERJanuary 27, 1992
K911326OBSTETRICAL VACUUM CUPAugust 14, 1991
K910652SPINAL TAP NEEDLEJuly 24, 1991
K911607GESCO UMBILI-CATHJune 11, 1991
K911215GESCO PER-Q-CATH NEEDLEJune 6, 1991
K910622GESCO PER-Q-CATH REPAIR KITMarch 29, 1991
K895942GESCO DUAL LUMEN PER-Q-CATH-DLJuly 2, 1990
K896041GESCO DUAL LUMEN UMBILICATH II-DLApril 17, 1990
K882647GESCO CATHETERIZATION TRAYSeptember 9, 1988
K872221DIALY-NATE SET & DIALY-NATE CATHETEROctober 13, 1987