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Taut, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K023261ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244December 13, 2002
K021731ADAPT OPEN ACCESS PORT, MODEL 41233August 8, 2002
K011018TAUT BALLOON CATHETER, MODEL 50640June 22, 2001
K003703TAUT-INSUFFLATION NEEDLEFebruary 22, 2001
K010007ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAPFebruary 22, 2001
K992904MINI-PORTOctober 5, 1999
K992907INTRADUCEROctober 5, 1999
K972112INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450December 1, 1997
K962003TUAT SPLATTER CONTROL SHIELD SCS-300July 18, 1996
K960883INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8March 20, 1996
K945486SPLATTER CONTROL SHIELDFebruary 28, 1995
K924981OPERATIVE CHOLANGIOGRAM CATHETERApril 6, 1993
K921934INTRADUCERJuly 15, 1992
K920040INTRADUCERFebruary 28, 1992
K875082O.P.C. INTRAVASCULAR CATHETERMarch 8, 1988
K830573PRE VUEMarch 29, 1983