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Target Therapeutics

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
70
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K964488DETACHABLE SILICONE BALLOON (DSB)April 21, 1998
K965071DETACHABLE SLICONE BALLOON (DSB)April 21, 1998
K964210RETRIEVER IIOctober 31, 1997
K971395GUGLIELMI DETACHABLE COIL (GDC), FIBERED PLATINUM COIL, .035 TYPE, BERENSTEIN LIQUID COIL, FIBERED PJuly 14, 1997
K965189SPINNAKERMarch 24, 1997
K964112BERENSTEIN COILFebruary 26, 1997
K963307GDC PATIENT RETURN ELECTTRODE MODEL 45021December 17, 1996
K962503GUGLIELMI DETACHABLE COILSeptember 20, 1996
K961923BERENSTEIN COILAugust 15, 1996
K960705GUGLIELMI DETACHABLE COILMay 21, 1996
K960806TURBO TRACKERMay 2, 1996
K955293FIBERED PLATINUM COIL, .035 TYPEFebruary 6, 1996
K951159FASGUIDESeptember 25, 1995
K951256DETACHABLE PLATINUM COIL (GUGLIELMI DETACHABLE COIL, GDC)September 8, 1995
K950069DASHER-14April 12, 1995
K935597FASGUIDE CATHETEROctober 18, 1994
K925813DIAGNOSTIC INTRAVASCULAR CATHETERMarch 23, 1994
K926243ANGIOGRAPHIC CATHETERAugust 16, 1993
K921247ZEPHYR INFUSION CATHETERJune 29, 1993
K925632BALT GUIDING CATHETERJune 29, 1993