# Diagnostic Technology, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 28 (1979–1991): 28 510(k) clearances
- Product codes: GKL (5), JHJ (3), JPK (3), GNP (2), LSR (1), GTQ (1), DHR (1), DCN (1), LJN (1), KRX (1), KTN (1), LSE (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
- K896378: Lyme-Check (TM) Test Kit (Nov 5, 1991)
- K903612: Ebv/EA-Check TM Test Kit (Oct 16, 1990)
- K890639: Resubmitted Ebv/Igm-Check Test Kit (Jun 20, 1989)
- K891542: Ebna-Check (TM) Test Kit (Jun 20, 1989)
- K890819: HSV-Check (TM) Test Kit (Jun 20, 1989)
- K871373: Ebv-Check (TM) Test Kit (Igg) (Jun 25, 1987)
- K864128: Chlamydia-Check (TM) Direct & Culture Confir. Kit (Apr 29, 1987)
- K863408: Ebv/Vca-Check (TM) Antigen Slides (Nov 28, 1986)

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