Siemens Burdick, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K915327ELITE II ELECTROCARDIOGRAPH,MODIFIEDOctober 9, 1992
K915225MEGACARTJuly 1, 1992
K915202INTERNAL MODEM FOR THE E560 ELECTROCARDIOGRAPHMay 15, 1992
K914969E350I ELECTROCARDIOGRAPHMarch 26, 1992
K913518TA620 TREADMILL CONTROLLEROctober 24, 1991
K910634DC200 DEFIBRILLATORJuly 24, 1991
K910867T600 TREADMILLMay 31, 1991