THYROGLOBULIN AUTOANTIBODY IMMUNOASSAY KIT— 510(k) K930777

Name: FDA 510(k) clearance K930777
Creator: U.S. Food and Drug Administration
Published: 1993-04-08

Substantially Equivalent

Nichols Institute

FDA 510(k) clearance K930777 for THYROGLOBULIN AUTOANTIBODY IMMUNOASSAY KIT, Substantially Equivalent on 1993-04-08. Applicant: Nichols Institute. Device class: 2.

Clearance details

Applicant: Nichols Institute
Product code: Code JNL
Device class: Class 2
Regulation: 21 CFR 866.5870
Advisory panel: Immunology
Date received: 1993-02-16
Decision date: 1993-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Juan Capistrano, CA, US

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