Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Thermo Fisher ScientificLabelled 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 Thermedics with 4 510(k) clearances. The most recent is a 510(k) clearance dated Sep 26, 1989: DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000.
| Sep 26, 1989 | DERMAPORT VASCULAR ACCESS DEVICE MODEL NO. 50-1000K894131 · DQY | 510(k) clearances |
| Sep 9, 1986 | PERITONEAL DIALYSIS CATHETERSK863128 · FJS | 510(k) clearances |
| Jan 9, 1986 | ACUTE PERITONEAL DIALYSIS CATHETERSK854966 · FKO | 510(k) clearances |
| Apr 15, 1985 | WOUND DRESSING MODEL ZB-6K850076 · NAD | 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