STANDARD & EXTENDED BLADE/NEEDLE/BALL; MODIFIED STANDARD & EXTENDED BLADE/NEEDLE— 510(k) K971187

Name: FDA 510(k) clearance K971187
Creator: U.S. Food and Drug Administration
Published: 1997-05-05

Substantially Equivalent

Aaron Medical Industries

FDA 510(k) clearance K971187 for STANDARD & EXTENDED BLADE/NEEDLE/BALL; MODIFIED STANDARD & EXTENDED BLADE/NEEDLE, Substantially Equivalent on 1997-05-05. Applicant: Aaron Medical Industries. Device class: 2.

Clearance details

Device name as filed: STANDARD & EXTENDED BLADE/NEEDLE/BALL;MODIFIED STANDARD & EXTENDED BLADE/NEEDLE
Applicant: Aaron Medical Industries
Product code: Code JOS
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1997-04-01
Decision date: 1997-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

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