ZEISS CATARACT SUITE MARKERLESS— 510(k) K141068

Name: FDA 510(k) clearance K141068
Creator: U.S. Food and Drug Administration
Published: 2014-09-09

Substantially Equivalent

Carl Zeiss Meditec, AG

FDA 510(k) clearance K141068 for ZEISS CATARACT SUITE MARKERLESS, Substantially Equivalent on 2014-09-09. Applicant: Carl Zeiss Meditec, AG. Device class: 2.

Clearance details

Applicant: Carl Zeiss Meditec, AG
Product code: Code HJO
Device class: Class 2
Regulation: 21 CFR 886.1850
Advisory panel: Ophthalmic
Date received: 2014-04-24
Decision date: 2014-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.