CHROMOTITRE E.I.A. RUBELLA IGG— 510(k) K872071

Name: FDA 510(k) clearance K872071
Creator: U.S. Food and Drug Administration
Published: 1987-08-24

Substantially Equivalent

Ismunit Istituto Immunologico Intaliano

FDA 510(k) clearance K872071 for CHROMOTITRE E.I.A. RUBELLA IGG, Substantially Equivalent on 1987-08-24. Applicant: Ismunit Istituto Immunologico Intaliano. Device class: 2.

Clearance details

Applicant: Ismunit Istituto Immunologico Intaliano
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1987-05-29
Decision date: 1987-08-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Roma, IT

Download summary PDF View on FDA.gov ↗

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