SUPER URINE ANALYZER SYSTEM— 510(k) K870526

Name: FDA 510(k) clearance K870526
Creator: U.S. Food and Drug Administration
Published: 1987-03-06

Substantially Equivalent

Kyoto Daiichi Kagaku Co., Ltd.

FDA 510(k) clearance K870526 for SUPER URINE ANALYZER SYSTEM, Substantially Equivalent on 1987-03-06. Applicant: Kyoto Daiichi Kagaku Co., Ltd.. Device class: 1.

Clearance details

Applicant: Kyoto Daiichi Kagaku Co., Ltd.
Product code: Code KQO
Device class: Class 1
Regulation: 21 CFR 862.2900
Advisory panel: Clinical Chemistry
Date received: 1987-02-06
Decision date: 1987-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kyoto, 601, JP

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