VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL— 510(k) K043315

Name: FDA 510(k) clearance K043315
Creator: U.S. Food and Drug Administration
Published: 2005-03-22

Substantially Equivalent

Vanguard Medical Concepts, Inc.

FDA 510(k) clearance K043315 for VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL, Substantially Equivalent on 2005-03-22. Applicant: Vanguard Medical Concepts, Inc.. Device class: Unclassified.

Clearance details

Applicant: Vanguard Medical Concepts, Inc.
Product code: Code NLQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 2004-12-01
Decision date: 2005-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakeland, FL, 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.