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Wiltek Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K990231WILTEK HOT BIOPSY FORCEPSApril 13, 1999
K922989WILTEK IRRIGAITON/ASPIRATION TUBE SETFebruary 15, 1994
K930419WILTEK BIOPSY FORCEPSJune 1, 1993
K914881WILTEK LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERJanuary 7, 1992
K914882WILTEK BALLOON CHOLANGIOGRAPHY CATHETERJanuary 7, 1992
K914131WILTEK ELECTROCAUTERY ADAPTORSeptember 25, 1991
K914132WILTEK ELECTROCAUTERY ACTIVE CORDSeptember 25, 1991
K912288WILTEK STANDARD CHOLANGIOGRAPHY CATHETERSeptember 23, 1991
K912122CHOLANGIOGRAPHY CATHETERSeptember 23, 1991
K910334ELECTROCAUTERY PROBEFebruary 21, 1991
K894861WILTEK PAPILLOTOMEDecember 21, 1989
K894867WILTEK E.R.C.P. CATHETERDecember 21, 1989
K894860WILTEK GASTRIC FEEDING TUBEDecember 21, 1989
K894870WILTEK NASAL BILIARY DRAINAGE SETDecember 21, 1989
K894863WILTEK CYTOLOGY BRUSHDecember 21, 1989
K894862WILTEK GRASPING FORCEPSDecember 21, 1989
K894871WILTEK BILIARY STENT SETDecember 21, 1989
K894869WILTEK POLYPECTOMY SNAREDecember 21, 1989
K894865WILTEK BALLOON STONE EXTRACTORDecember 21, 1989
K894868WILTEK VARICES INJECTION NEEDLEDecember 21, 1989