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Leocor, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K924110LEOCOR CORFLO PUMP -- MODIFICATIONSeptember 1, 1992
K911270LEOCOR GUIDING CATHETERJanuary 17, 1992
K900350LEOCOR CORFLO(TM) PUMPJuly 17, 1990