KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT— 510(k) K896440

Name: FDA 510(k) clearance K896440
Creator: U.S. Food and Drug Administration
Published: 1990-02-16

Substantially Equivalent

Kenlor Industries, Inc.

FDA 510(k) clearance K896440 for KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KIT, Substantially Equivalent on 1990-02-16. Applicant: Kenlor Industries, Inc.. Device class: 1.

Clearance details

Applicant: Kenlor Industries, Inc.
Product code: Code JIR
Device class: Class 1
Regulation: 21 CFR 862.1645
Advisory panel: Clinical Chemistry
Date received: 1989-11-09
Decision date: 1990-02-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Huntington Beach, CA, US

Download summary PDF View on FDA.gov ↗

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