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Dey Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K972778DEY VIAL SODIUM CHLORIDE 3%October 8, 1997
K910239NEBU-SOL METERED DOSE DISPENSER (TM)May 22, 1991
K880411DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILEFebruary 29, 1988
K875011DEY-PAK PURIFIED WATER, USP, STERILEJanuary 22, 1988
K875024DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USPJanuary 22, 1988
K831532OCULAR IRRIGATING CANNULAJuly 12, 1983