# Diatech, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 17 (1984–1988): 17 510(k) clearances
- Product codes: JPA (5), GGP (3), KQJ (2), GGW (1), GIS (1), JPK (1), GGN (1), GJS (1), GIR (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
- K881685: Fibrinogentest-O (Aug 9, 1988)
- K854938: Coascreener/Diascreenerblood Plasma Timing Inst. (Mar 12, 1986)
- K854089: Diatimer-1 Blood Plasma Clot Timing Instrument (Jan 6, 1986)
- K854090: Diatimer-2 Blood Plasma Clot Timing Instrument (Jan 6, 1986)
- K842286: Dia T1, T2 & T3 (Sep 11, 1984)
- K841366: Dia Fibrin (Jun 1, 1984)
- K841523: Owren's Veronal Bufferr (Jun 1, 1984)
- K841462: Heparin Coagulation Control Plasma 1- (Jun 1, 1984)

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