Stoeckert Instrumente

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002273STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAEJanuary 29, 2001
K001961STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAEJanuary 25, 2001
K002118STOCKERT COMPACT SYSTEM VERSION 2.0August 9, 2000
K992635INTERFACE MODULE IDDDDecember 20, 1999
K990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSNovember 23, 1999
K982014STOCKERT COMPACT SYSTEMSeptember 4, 1998
K972321S3 MAST PUMPFebruary 27, 1998
K971520S3 CYCLIC RPM CONTROLSeptember 10, 1997
K962320S3 CARDIOPLEGIA CONTROLJanuary 10, 1997
K955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMERFebruary 22, 1996
K955038STOCKERT S3 DOUBLE HEAD PUMP MODULEFebruary 21, 1996
K950990STOCKERT S3 ROLLER PUMP MODULE STOCKERT S3 CONSOLEJanuary 19, 1996
K812049STOCKERT CARDIAC PACING ELECTRODESMarch 18, 1982