MAGIC TM 125I T3 UPTAKE RADIOASSAY— 510(k) K831613

Name: FDA 510(k) clearance K831613
Creator: U.S. Food and Drug Administration
Published: 1983-08-11

Substantially Equivalent

Corning Medical & Scientific

FDA 510(k) clearance K831613 for MAGIC TM 125I T3 UPTAKE RADIOASSAY, Substantially Equivalent on 1983-08-11. Applicant: Corning Medical & Scientific. Device class: 2.

Clearance details

Applicant: Corning Medical & Scientific
Product code: Code KHQ
Device class: Class 2
Regulation: 21 CFR 862.1715
Advisory panel: Clinical Chemistry
Date received: 1983-05-19
Decision date: 1983-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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