LEMAITRE RETROGRADE VALVULOTOME— 510(k) K924171

Name: FDA 510(k) clearance K924171
Creator: U.S. Food and Drug Administration
Published: 1993-02-16

Substantially Equivalent

Vascutech, Inc.

FDA 510(k) clearance K924171 for LEMAITRE RETROGRADE VALVULOTOME, Substantially Equivalent on 1993-02-16. Applicant: Vascutech, Inc.. Device class: 2.

Clearance details

Applicant: Vascutech, Inc.
Product code: Code MGZ
Device class: Class 2
Regulation: 21 CFR 870.4885
Advisory panel: Cardiovascular
Date received: 1992-08-18
Decision date: 1993-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

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K992933 — LEMAITRE IRRIGATION CATHETER2000-03-08
K992934 — LEMAITRE VENOUS THROMBECTOMY CATHETER2000-03-01
K992940 — LEMAITRE BALLOON CATHETER WITH IRRIGATION2000-02-22

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