Target Therapeutics

FDA Regulatory Profile

Target Therapeutics appears in FDA public data with 0 recalls, 70 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 21, 1998.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K964488DETACHABLE SILICONE BALLOON (DSB)Apr 21, 1998
K965071DETACHABLE SLICONE BALLOON (DSB)Apr 21, 1998
K964210RETRIEVER IIOct 31, 1997
K971395GUGLIELMI DETACHABLE COIL (GDC), FIBERED PLATINUM COIL, .035 TYPE, BERENSTEIN LIQUID COIL, FIBERED PJul 14, 1997
K965189SPINNAKERMar 24, 1997
K964112BERENSTEIN COILFeb 26, 1997
K963307GDC PATIENT RETURN ELECTTRODE MODEL 45021Dec 17, 1996
K962503GUGLIELMI DETACHABLE COILSep 20, 1996
K961923BERENSTEIN COILAug 15, 1996
K960705GUGLIELMI DETACHABLE COILMay 21, 1996
K960806TURBO TRACKERMay 2, 1996
K955293FIBERED PLATINUM COIL, .035 TYPEFeb 6, 1996
K951159FASGUIDESep 25, 1995
K951256DETACHABLE PLATINUM COIL (GUGLIELMI DETACHABLE COIL, GDC)Sep 8, 1995
K950069DASHER-14Apr 12, 1995
K935597FASGUIDE CATHETEROct 18, 1994
K925813DIAGNOSTIC INTRAVASCULAR CATHETERMar 23, 1994
K926243ANGIOGRAPHIC CATHETERAug 16, 1993
K925632BALT GUIDING CATHETERJun 29, 1993
K921247ZEPHYR INFUSION CATHETERJun 29, 1993