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 Boston 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 15, 2026, FDA's public records list Guidant Corporation Cardiac Surgery with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 8, 2008: HEARTSTRING III PROXIMAL SEAL SYSTEM.
| Feb 8, 2008 | HEARTSTRING III PROXIMAL SEAL SYSTEMK080169 · DXC | 510(k) clearances |
| Jul 28, 2004 | GUIDANT MICROWAVE ABLATION SYSTEMK041340 · NEY | 510(k) clearances |
| Feb 20, 2003 | ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400K023630 · GCJ | 510(k) clearances |
| Feb 14, 2003 | GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEMK024071 · NHW | 510(k) clearances |
| Nov 12, 2002 | ESSEX DISSECTION CANNULA, MODEL SXD-1100, ESSEX DISSECTION TIP, MODEL SXD-1200K023629 · GCJ | 510(k) clearances |
| Aug 28, 2002 | VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002K022718 · GEI | 510(k) clearances |
| May 24, 2002 | SYNCRUS INTERNAL CARDIOVERSION SYSTEMK020701 · NHW | 510(k) clearances |
| Feb 20, 2002 | VASOVIEW 5 HARVESTING CANNULAK020143 · HET | 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
