# Diagnon Corp.

- Location (FDA's records): Laurel, MD
- FDA decisions: 6 (1983–1986): 6 510(k) clearances
- Product codes: CDD (2), CGN (1), LIO (1), JSN (1), GQL (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
- K860967: Virtran Viral Transporter (Modified) (Apr 4, 1986)
- K851635: Diagnon Herpes Immunoperoxidase Typing Test (Oct 10, 1985)
- K851377: Diagnon Monocombo Vitam. B12[57CO]/Folate[125I] RA (Aug 21, 1985)
- K851378: Virtran Viral Tranporter (Jun 21, 1985)
- K841302: Diagnon Folate 125I Ria Kit (Jun 22, 1984)
- K832717: Diagnon B12 57CO Ria Kit (Dec 8, 1983)

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