CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US— 510(k) K072643

Name: FDA 510(k) clearance K072643
Creator: U.S. Food and Drug Administration
Published: 2007-11-16

Substantially Equivalent

Olympus Corporation

FDA 510(k) clearance K072643 for CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US, Substantially Equivalent on 2007-11-16. Applicant: Olympus Corporation. Device class: 2.

Clearance details

Applicant: Olympus Corporation
Product code: Code KZN
Device class: Class 2
Regulation: 21 CFR 872.3661
Advisory panel: Dental
Date received: 2007-09-18
Decision date: 2007-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tokyo, JP

Download summary PDF View on FDA.gov ↗

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