URIC ACID TEST, BMC AUTOFLO— 510(k) K770272

Name: FDA 510(k) clearance K770272
Creator: U.S. Food and Drug Administration
Published: 1977-03-01

Substantially Equivalent

Boehringer Mannheim Corp.

FDA 510(k) clearance K770272 for URIC ACID TEST, BMC AUTOFLO, Substantially Equivalent on 1977-03-01. Applicant: Boehringer Mannheim Corp.. Device class: 1.

Clearance details

Applicant: Boehringer Mannheim Corp.
Product code: Code KNK
Device class: Class 1
Regulation: 21 CFR 862.1775
Advisory panel: Clinical Chemistry
Date received: 1977-02-14
Decision date: 1977-03-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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