VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE— 510(k) K011832

Name: FDA 510(k) clearance K011832
Creator: U.S. Food and Drug Administration
Published: 2001-12-21

Substantially Equivalent

Vanguard Medical Concepts, Inc.

FDA 510(k) clearance K011832 for VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE, Substantially Equivalent on 2001-12-21. Applicant: Vanguard Medical Concepts, Inc.. Device class: 2.

Clearance details

Applicant: Vanguard Medical Concepts, Inc.
Product code: Code NMF
Device class: Class 2
Regulation: 21 CFR 870.4450
Advisory panel: Cardiovascular
Date received: 2001-06-12
Decision date: 2001-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakeland, FL, US

Download summary PDF View on FDA.gov ↗

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