Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Electromek Diagnostic Systems, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Feb 13, 1991: G.E. DXD 325/350/350II/DXD 525/525II GENERATORS.
| Feb 13, 1991 | G.E. DXD 325/350/350II/DXD 525/525II GENERATORSK902986 · IZO | 510(k) clearances |
| Dec 26, 1990 | G.E. DXS 350/550/650/650II SINGLE PHASE GENERATORSK902987 · IZO | 510(k) clearances |
| Dec 19, 1990 | G.E. MST 625/625II/MST 1050/1050II THREE PHASE GENK902985 · IZO | 510(k) clearances |
| Dec 19, 1990 | G.E. MSI 850/850II/1250 THREE PHASE GENERATORSK902988 · IZO | 510(k) clearances |
| Nov 13, 1990 | G.E. POLARIX II C-ARMK902982 · JAA | 510(k) clearances |
| Nov 7, 1990 | G.E. FLUOROCON 300 IMAGING SYSTEMK902981 · JAA | 510(k) clearances |
| Nov 6, 1990 | SIEMEN'S SIREMOBILE II C-ARMK902983 · JAA | 510(k) clearances |
| Oct 29, 1990 | G.E. 48-4 CEILING TUBEHANGERK902791 · KPR | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
