# Diagnostica, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1978–2001): 12 510(k) clearances
- Product codes: DEW (3), GRP (1), LHT (1), DEH (1), DGQ (1), KHE (1), JXB (1), DFH (1), JBX (1), JWT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K002756: Ease-a-Cult (Feb 23, 2001)
- K823348: H. Influenza B Antisera for Cie (Dec 28, 1982)
- K812434: Diagnostic Kits & Kit Components (Sep 23, 1981)
- K800398: Paracontrol Abnormal Immunoglobulin Cont (Mar 12, 1980)
- K791283: Anti-Human Lambda Serum (Nov 27, 1979)
- K791281: Anti-Human Igg Serum (Nov 27, 1979)
- K791284: Anti-Human Kappa Serum (Nov 27, 1979)
- K791282: Anti-Human Serum (Oct 17, 1979)

Source page: https://510kreport.com/company/diagnostica