# Electromek Diagnostic Systems, Inc.

- Location (FDA's records): Troy, IL
- FDA decisions: 11 (1990–1991): 11 510(k) clearances
- Product codes: IZO (4), JAA (4), KPR (1), IZL (1), IXR (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
- K902986: G.E. DXD 325/350/350II/DXD 525/525II Generators (Feb 13, 1991)
- K902987: G.E. DXS 350/550/650/650II Single Phase Generators (Dec 26, 1990)
- K902985: G.E. MST 625/625II/MST 1050/1050II Three Phase Gen (Dec 19, 1990)
- K902988: G.E. Msi 850/850II/1250 Three Phase Generators (Dec 19, 1990)
- K902982: G.E. Polarix II C-Arm (Nov 13, 1990)
- K902981: G.E. Fluorocon 300 Imaging System (Nov 7, 1990)
- K902983: Siemen's Siremobile II C-Arm (Nov 6, 1990)
- K902791: G.E. 48-4 Ceiling Tubehanger (Oct 29, 1990)

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