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Company · US

Dey Laboratories, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1997. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
CAF	Nebulizer (Direct Patient Interface)	2
CCQ	Nebulizer, Medicinal, Non-Ventilatory (Atomizer)	2
BSY	Catheters, Suction, Tracheobronchial	1
HMX	Cannula, Ophthalmic	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Oct 8, 1997	K972778	DEY VIAL SODIUM CHLORIDE 3% Dey Laboratories, Inc.	CAF
May 22, 1991	K910239	NEBU-SOL METERED DOSE DISPENSER (TM) Dey Laboratories, Inc.	BSY
Feb 29, 1988	K880411	DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE Dey Laboratories, Inc.	CAF
Jan 22, 1988	K875024	DEY-PAK AND DEY-VIAL SODIUM CHLORIDE SOLUTION, USP Dey Laboratories, Inc.	CCQ
Jan 22, 1988	K875011	DEY-PAK PURIFIED WATER, USP, STERILE Dey Laboratories, Inc.	CCQ
Jul 12, 1983	K831532	OCULAR IRRIGATING CANNULA Dey Laboratories, Inc.	HMX

Latest recalls

Date	Firm and product	Code	Linked 510(k)
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