IMMOPHASE D-TE 3 RADIOIMMUNOASSAY— 510(k) K833406

Name: FDA 510(k) clearance K833406
Creator: U.S. Food and Drug Administration
Published: 1984-01-24

Substantially Equivalent

Corning Medical & Scientific

FDA 510(k) clearance K833406 for IMMOPHASE D-TE 3 RADIOIMMUNOASSAY, Substantially Equivalent on 1984-01-24. Applicant: Corning Medical & Scientific. Device class: 1.

Clearance details

Applicant: Corning Medical & Scientific
Product code: Code CGF
Device class: Class 1
Regulation: 21 CFR 862.1280
Advisory panel: Clinical Chemistry
Date received: 1983-09-30
Decision date: 1984-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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