# Intl. Diagnostic, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1978–1984): 6 510(k) clearances
- Product codes: JHJ (3), DCN (1), DHR (1), LCX (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
- K841853: Preg-Beta One Hour Tube Test (Jun 22, 1984)
- K840833: Preg Beta Blus Slide (May 30, 1984)
- K834584: Nabi CRP-Q.S. Test (Feb 27, 1984)
- K840005: Nabi RF-Q.S. Test (Feb 13, 1984)
- K802343: Pregna B-Anti Human Chorionic Gonadotro (Oct 10, 1980)
- K780321: Pregnancy Test Kit, Over-the-Counter (Apr 4, 1978)

Source page: https://510kreport.com/company/intl-diagnostic