UBAS MANUAL METHOD AND UBAS AUTOMATED METHOD— 510(k) K980525

Name: FDA 510(k) clearance K980525
Creator: U.S. Food and Drug Administration
Published: 1998-04-15

Substantially Equivalent

Marukin Shoyu Co., Ltd.

FDA 510(k) clearance K980525 for UBAS MANUAL METHOD AND UBAS AUTOMATED METHOD, Substantially Equivalent on 1998-04-15. Applicant: Marukin Shoyu Co., Ltd.. Device class: 2.

Clearance details

Applicant: Marukin Shoyu Co., Ltd.
Product code: Code KWX
Device class: Class 2
Regulation: 21 CFR 862.1187
Advisory panel: Clinical Chemistry
Date received: 1998-02-11
Decision date: 1998-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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