# Antibodies, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 16 (1977–1989): 16 510(k) clearances
- Product codes: CFN (3), KLQ (1), DHN (1), CGR (1), DNJ (1), LCS (1), GTZ (1), CDP (1), DJB (1), KLB (1), CZW (1), KHW (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
- K890774: Giardeia (TM) (Apr 4, 1989)
- K843590: Detect-a-Strep (Oct 30, 1984)
- K822892: Cortisol Ria Kit (Nov 1, 1982)
- K812749: Ultra-Dig (Oct 19, 1981)
- K812314: Crithidna Anti-Dna Test Kit (Sep 1, 1981)
- K802877: Amikacin Ria Kit (Dec 19, 1980)
- K800743: Tobramycin Ria Kit (Apr 16, 1980)
- K791217: TSH Ria Kit (Sep 4, 1979)

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