BURR, CORNEAL, BATTERY-POWERED— 510(k) K950520

Name: FDA 510(k) clearance K950520
Creator: U.S. Food and Drug Administration
Published: 1995-05-02

Substantially Equivalent

Aaron Medical Industries

FDA 510(k) clearance K950520 for BURR, CORNEAL, BATTERY-POWERED, Substantially Equivalent on 1995-05-02. Applicant: Aaron Medical Industries. Device class: 1.

Clearance details

Applicant: Aaron Medical Industries
Product code: Code HOG
Device class: Class 1
Regulation: 21 CFR 886.4070
Advisory panel: Ophthalmic
Date received: 1995-02-06
Decision date: 1995-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Petersburg, FL, US

Download summary PDF View on FDA.gov ↗

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