# Dey Laboratories, Inc.

- Location (FDA's records): Concord, CA
- FDA decisions: 6 (1983–1997): 6 510(k) clearances
- Product codes: CCQ (2), CAF (2), BSY (1), HMX (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Armour Pharmaceutical Co.: 2 (https://510kreport.com/company/armour-pharmaceutical)

## Firms that cite its devices most
- Pari Innovative Manufacturers, Inc.: 1 (https://510kreport.com/company/pari-innovative-manufacturers)
- Pharmacaribe: 1 (https://510kreport.com/company/pharmacaribe)
- Nephron Pharmaceuticals Corp.: 1 (https://510kreport.com/company/nephron-pharmaceuticals)

## Its most-cited devices
- K972778: Dey Vial Sodium Chloride 3% (1997), cited by 3
- K880411: Dey-Vial Sodium Chloride Solution, Usp, Sterile (1988), cited by 1

## Recent decisions
- K972778: Dey Vial Sodium Chloride 3% (Oct 8, 1997)
- K910239: Nebu-Sol Metered Dose Dispenser (TM) (May 22, 1991)
- K880411: Dey-Vial Sodium Chloride Solution, Usp, Sterile (Feb 29, 1988)
- K875024: Dey-Pak and Dey-Vial Sodium Chloride Solution, Usp (Jan 22, 1988)
- K875011: Dey-Pak Purified Water, Usp, Sterile (Jan 22, 1988)
- K831532: Ocular Irrigating Cannula (Jul 12, 1983)

Source page: https://510kreport.com/company/dey-laboratories