ALLEGRO (TM) FERRITIN IMMUNOASSAY SYSTEM— 510(k) K874572

Name: FDA 510(k) clearance K874572
Creator: U.S. Food and Drug Administration
Published: 1987-12-02

Substantially Equivalent

Nichols Institute Diagnostics

FDA 510(k) clearance K874572 for ALLEGRO (TM) FERRITIN IMMUNOASSAY SYSTEM, Substantially Equivalent on 1987-12-02. Applicant: Nichols Institute Diagnostics. Device class: 2.

Clearance details

Applicant: Nichols Institute Diagnostics
Product code: Code DBF
Device class: Class 2
Regulation: 21 CFR 866.5340
Advisory panel: Immunology
Date received: 1987-11-05
Decision date: 1987-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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