MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626— 510(k) K022238

Name: FDA 510(k) clearance K022238
Creator: U.S. Food and Drug Administration
Published: 2002-10-09

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K022238 for MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626, Substantially Equivalent on 2002-10-09. Applicant: Medtronic Vascular. Device class: 1.

Clearance details

Applicant: Medtronic Vascular
Product code: Code DWS
Device class: Class 1
Regulation: 21 CFR 870.4500
Advisory panel: Cardiovascular
Date received: 2002-07-11
Decision date: 2002-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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