Leocor, Inc.

FDA Regulatory Profile

Leocor, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 1, 1992.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K924110LEOCOR CORFLO PUMP -- MODIFICATIONSep 1, 1992
K911270LEOCOR GUIDING CATHETERJan 17, 1992
K900350LEOCOR CORFLO(TM) PUMPJul 17, 1990