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 13, 2026, FDA's public records list Cynergy with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 1, 1981: SIEMENS MODEL 146-146A EXTERNAL PULSE G.
| Date | Record | Source |
|---|---|---|
| Apr 1, 1981 | SIEMENS MODEL 146-146A EXTERNAL PULSE GK810566 · DTE | 510(k) clearances |
| Sep 16, 1980 | CYNERGY MODEL 184K801596 · DTE | 510(k) clearances |
| Jan 31, 1980 | CYNERGY MODEL 182K792536 · DTE | 510(k) clearances |
| Nov 30, 1979 | PACESETTER MODEL 350K792223 · DTE | 510(k) clearances |
| Sep 27, 1978 | ERM-101K781407 · DRT | 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
