Schneider Intl., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
22
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K925406BILIARY ENDOPROSTHESES W/UNISTEP DELIVERY SYSTEMJanuary 11, 1995
K931577SCHNEIDER MAGNUM PERIPHERAL RECANALIZATION GUIDEWIJune 23, 1993
K926271SCHNEIDER MATCH-35 PERCUTANEOUS TRANSLUMINAL ANGIOJune 7, 1993
K926003SCHNEIDER SOFTIP SST ANGIOGRAPHIC (DIAG) CATHETERJune 7, 1993
K925804SCHNEIDER HYDRO-SIL GUIDEWIREFebruary 12, 1993
K924591SCHNEIDER SOLID-7 SOPTIP GUIDING CATHETERDecember 8, 1992
K921856TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.July 21, 1992
K921943SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO (PTA) BALJune 17, 1992
K920157SCHNEIDER 8 FR. STAMINA(TM) GUIDING CATHETERMarch 16, 1992
K915349PTA BALLOON CATHETERFebruary 11, 1992
K914009SCHNEIDER SOFTIP(R) A+(TM) ANGIOGRAPHIC CATHETERDecember 6, 1991
K913297SCHNEIDER MATCH-35(TM) PERCU TRANS ANGIOPLAS CATHOctober 10, 1991
K912156SCHNEIDER MAGNUM PERIPHERAL RECANAL GUIDEWIRESeptember 6, 1991
K912317SCHNEIDER MONORAIL 421 PERCU TRANS ANGIO PTA CATHAugust 22, 1991
K911547MAGNUM-MEIER RECANALIZATION GUIDEWIREJuly 5, 1991
K911196SCHNEIDER TOTAL CROSS .021 PERCU TRANS ANGIO (PTA)June 10, 1991
K910259SCHNEIDER MAGNARAIL PROBING CATHETERApril 18, 1991
K902587SCHNEIDER MONORAIL-GEX(TM) GUIDEWIRE EXCHANGE CATHDecember 3, 1990
K902091SCHNEIDER MONORAIL(TM) SOFTRAC-PTA(TM) CATHETERSeptember 26, 1990
K897082SCHNEIDER SIDEKICK MONORAIL Y-CONNECTORMarch 6, 1990