# Immuno-Products Industries

- Location (FDA's records): Mchenry, IL
- FDA decisions: 12 (1981–1985): 12 510(k) clearances
- Product codes: DHN (2), LJM (2), GMS (2), DBL (1), DHC (1), KTL (1), JZO (1), DBE (1), DBM (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
- K853122: Immuno-Prod Ind Fluore Trepone Antibody Absorped (Sep 19, 1985)
- K852230: Ana/Lite-RL Test System (Jul 10, 1985)
- K852231: Ana/Lite-Hep-2 Test System (Jul 10, 1985)
- K843613: Fluorescent Treponemel Antibody-Absorb (Oct 31, 1984)
- K831054: Antinuclear Antibody Tissue Culture Sub (Apr 27, 1983)
- K830652: Anti N Dna-HCP (Mar 24, 1983)
- K821576: Antinuclear Antibody Screen Flouresc (Jun 10, 1982)
- K810985: Antinuclear Antibody Immunofluorescent (May 1, 1981)

Source page: https://510kreport.com/company/immuno-products-industries