ALEXIS WOUND RETRACTOR— 510(k) K062907

Name: FDA 510(k) clearance K062907
Creator: U.S. Food and Drug Administration
Published: 2007-01-09

Substantially Equivalent

Applied Medical Resources

FDA 510(k) clearance K062907 for ALEXIS WOUND RETRACTOR, Substantially Equivalent on 2007-01-09. Applicant: Applied Medical Resources. Device class: 2.

Clearance details

Applicant: Applied Medical Resources
Product code: Code KGW
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 2006-09-27
Decision date: 2007-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rancho Santa, CA, US

Download summary PDF View on FDA.gov ↗

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