Hancock Laboratories, Inc.

FDA Regulatory Profile

Hancock Laboratories, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 9, 1980.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K801885HANCOCK * OBTURATORSSeptember 9, 1980
K800703MODIFIED CATHETER PACKAGEApril 8, 1980
K800122HANCOCK AORTIC PUNCHFebruary 1, 1980
K790534MERSILENE SUTURESMarch 26, 1979
K780568DURAN FLEXIBLE RINGMay 26, 1978