# Ventrex Laboratories, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 82 (1979–1992): 82 510(k) clearances
- Product codes: DHB (18), DGC (12), JHI (4), JLW (4), KIT (2), CDP (2), CFP (2), KHQ (2), GTZ (2), JIT (2), KQN (2), CDX (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Bio-Rad Laboratories, Inc.: 1 (https://510kreport.com/company/bio-rad-laboratories)

## Its most-cited devices
- K832218: Allergen Control Inhalent (1983), cited by 1

## Recent decisions
- K914554: Specific Ige Eia-Turbo Assay (Mar 13, 1992)
- K913833: Ventrex Allergen Disc (Feb 21, 1992)
- K913434: Ventrex Coated Tube Intact PTH (Oct 25, 1991)
- K905612: Ventrex Coated Tube Ige Radioimmunoassay (Feb 21, 1991)
- K905636: Ventrex Coated Tube Ige Enzyme Immunoassay (Feb 7, 1991)
- K905247: SHBG Irma Kit (Jan 17, 1991)
- K904330: Turbo-Rast Specific Ige Assay (Dec 7, 1990)
- K903000: Turbo-Rast Specific Ige Assay (Jul 31, 1990)

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