SUTURE REMOVAL KIT— 510(k) K810685

Name: FDA 510(k) clearance K810685
Creator: U.S. Food and Drug Administration
Published: 1981-03-26

Substantially Equivalent

Medical Action Industries, Inc.

FDA 510(k) clearance K810685 for SUTURE REMOVAL KIT, Substantially Equivalent on 1981-03-26. Applicant: Medical Action Industries, Inc.. Device class: 1.

Clearance details

Applicant: Medical Action Industries, Inc.
Product code: Code GEN
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-03-13
Decision date: 1981-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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