LEMAITRE RETROGRADE VALVULOTOME— 510(k) K924171

Substantially Equivalent

Vascutech, Inc.

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

Clearance details

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

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