Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of GE HealthCareLabelled by claude-sonnet-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 15, 2026, FDA's public records list CGR Medical with 20 510(k) clearances. The most recent is a 510(k) clearance dated Dec 17, 1984: PRESTILIX 1690.
| Dec 17, 1984 | PRESTILIX 1690K843926 · IXR | 510(k) clearances |
| Nov 8, 1984 | STENOSCOPK843235 · JAA | 510(k) clearances |
| Nov 5, 1984 | SUSPENSION 7K843985 · | 510(k) clearances |
| Jun 5, 1984 | MAXIMAX - 4K841649 · IZP | 510(k) clearances |
| May 9, 1984 | SONEL 3000AK833223 · IYO | 510(k) clearances |
| Dec 29, 1983 | PHASIX-HIGH FREQUENCY GENERATORK834306 · ITY | 510(k) clearances |
| Dec 29, 1983 | ORIONK833941 · IYE | 510(k) clearances |
| Dec 16, 1983 | PROCESS 100 STK833846 · IZO | 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
