Dey Laboratories, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Dey Laboratories, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1997. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dey Laboratories, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Oct 08, 1997
DEY VIAL SODIUM CHLORIDE 3%
Anesthesiology
75d
Cleared
May 22, 1991
NEBU-SOL METERED DOSE DISPENSER (TM)
Anesthesiology
120d
Cleared
Feb 29, 1988
DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE
Anesthesiology
28d
Cleared
Jan 22, 1988
DEY-PAK PURIFIED WATER, USP, STERILE
Anesthesiology
49d
Cleared
Jan 22, 1988
DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP
Anesthesiology
49d
Cleared
Jul 12, 1983
OCULAR IRRIGATING CANNULA
Ophthalmic
60d