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Lafayette Pharmacal, Inc.

FDA Regulatory Profile

Lafayette Pharmacal, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 26, 1993.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K931896PRO-FLO SYSTEMAugust 26, 1993
K884379MAGLINTE ENTEROCLYSIS CATHETERFebruary 28, 1989
K881609SITZMARKSJuly 8, 1988
K860441ENTROKIT WITH MAGLINTE CATHETERMarch 12, 1986

FDA data resources