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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list SurVivaLink with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 1, 2002: FIRSTSAVE STAR BIPHASIC, MODEL 9210/9200.
| Feb 1, 2002 | FIRSTSAVE STAR BIPHASIC, MODEL 9210/9200K011901 · MKJ | 510(k) clearances |
| Feb 22, 2001 | FIRSTSAVE BIPHASIC MODEL #9200 AND 9210K010214 · MKJ | 510(k) clearances |
| Dec 10, 1999 | SURVIVALINK MULTIFUNCTIONAL ELECTRODE (SVL-9630)K993072 · MKJ | 510(k) clearances |
| Jan 25, 1999 | FIRSTSAVE BIPHASIC MODELS 9200 AND 9210K982264 · MKJ | 510(k) clearances |
| Jul 1, 1997 | V2K970481 · LDD | 510(k) clearances |
| Jun 23, 1997 | SVL-9130 DEFIBRILLATION ELECTRODEK971149 · MKJ | 510(k) clearances |
| Feb 9, 1995 | VIVALINK AED DEFIBRILLATORK940445 · MKJ | 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
