LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER— 510(k) K023688

Name: FDA 510(k) clearance K023688
Creator: U.S. Food and Drug Administration
Published: 2003-01-30

Substantially Equivalent

LeMaitre Vascular, Inc.

FDA 510(k) clearance K023688 for LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPER, Substantially Equivalent on 2003-01-30. Applicant: LeMaitre Vascular, Inc.. Device class: 1.

Clearance details

Applicant: LeMaitre Vascular, Inc.
Product code: Code GAF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 2002-11-01
Decision date: 2003-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.