EZ-SCOPE AN, EZ-SCOPE LIGHT— 510(k) K022342

Name: FDA 510(k) clearance K022342
Creator: U.S. Food and Drug Administration
Published: 2002-10-09

Substantially Equivalent

Anzai Medical Co., Ltd.

FDA 510(k) clearance K022342 for EZ-SCOPE AN, EZ-SCOPE LIGHT, Substantially Equivalent on 2002-10-09. Applicant: Anzai Medical Co., Ltd.. Device class: 1.

Clearance details

Applicant: Anzai Medical Co., Ltd.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 2002-07-18
Decision date: 2002-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brookeville, MD, US

Download summary PDF View on FDA.gov ↗

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