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Guidant

Medical device maker in United States, part of Boston Scientific. FDA records under 2 spellings of its name, each linked to the record.

  • 510(k) clearances: 86

Latest Records

Newest first across sources; each opens the record
DateRecordSource
Jul 27, 2006FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05K061865 · NEY510(k) clearances
Jun 22, 2006HI-TORQUE WHISPER VIEW GUIDE WIREK061453 · DQX510(k) clearances
May 30, 2006HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIREK060449 · DQX510(k) clearances
Apr 12, 2006OMNILINK .035 BILIARY STENT SYSTEMK053459 · FGE510(k) clearances
Mar 6, 2006RX HERCULINK ELITE BILIARY STENT SYSTEMK053454 · FGE510(k) clearances
Mar 3, 2006ACUITY STEERABLE STYLET ACCESSORYK053019 · DRB510(k) clearances
Feb 13, 2006EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.K052965 · DRB510(k) clearances
Sep 21, 2005GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000K052274 · GEI510(k) clearances

Names and Identifiers

Appears as
Guidant Corp.Guidant Corporation

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

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.