B2-MICROGLOBULIN RADIOIMMUNOASSAY— 510(k) K920300

Name: FDA 510(k) clearance K920300
Creator: U.S. Food and Drug Administration
Published: 1992-03-17

Substantially Equivalent

Nichols Institute

FDA 510(k) clearance K920300 for B2-MICROGLOBULIN RADIOIMMUNOASSAY, Substantially Equivalent on 1992-03-17. Applicant: Nichols Institute. Device class: 2.

Clearance details

Applicant: Nichols Institute
Product code: Code JZG
Device class: Class 2
Regulation: 21 CFR 866.5630
Advisory panel: Immunology
Date received: 1992-01-22
Decision date: 1992-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Juan Capistrano, CA, US

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