PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36— 510(k) K070270

Name: FDA 510(k) clearance K070270
Creator: U.S. Food and Drug Administration
Published: 2007-11-05

Substantially Equivalent

Kirchner & Wilhelm GmbH + Co.Kg

FDA 510(k) clearance K070270 for PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36, Substantially Equivalent on 2007-11-05. Applicant: Kirchner & Wilhelm GmbH + Co.Kg. Device class: 2.

Clearance details

Applicant: Kirchner & Wilhelm GmbH + Co.Kg
Product code: Code HLJ
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 2007-01-29
Decision date: 2007-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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