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 15, 2026, FDA's public records list Conway Stuart Medical with 10 510(k) clearances. The most recent is a 510(k) clearance dated Apr 18, 2000: CSM STRETTA SYSTEM.
| Apr 18, 2000 | CSM STRETTA SYSTEMK000245 · GEI | 510(k) clearances |
| Feb 14, 2000 | SECCA TUBULAR ELECTRODE DEVICE, MODEL A4000K000170 · GEI | 510(k) clearances |
| Oct 27, 1999 | TUBULAR ELECTRODE DEVICEK992542 · GEI | 510(k) clearances |
| Sep 14, 1999 | CSM STRETTA CONTROL MODULE ELECTROSURGICAL GENERATOR, MODEL S400K991529 · GEI | 510(k) clearances |
| Aug 13, 1999 | CONWAY STUART MODEL 100 IRRIGATION PUMP & ACCESSORIESK990724 · GCJ | 510(k) clearances |
| Jul 14, 1999 | STRETTA INFLATABLE BASKET CATHETER ELECTRODE WITH ASPIRATIONK991291 · GEI | 510(k) clearances |
| Mar 23, 1999 | CONWAY STUART MEDICAL MODEL C4 ELECTROSURGICAL GENERATORK983986 · GEI | 510(k) clearances |
| Dec 3, 1998 | ELECTROSURGICAL INFLATABLE BASKET ELECTRODESK983116 · GEI | 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
