VITAMIN B12 FOLATE RADIOASSAY— 510(k) K802037

Name: FDA 510(k) clearance K802037
Creator: U.S. Food and Drug Administration
Published: 1980-11-21

Substantially Equivalent

Corning Medical & Scientific

FDA 510(k) clearance K802037 for VITAMIN B12 FOLATE RADIOASSAY, Substantially Equivalent on 1980-11-21. Applicant: Corning Medical & Scientific. Device class: 1.

Clearance details

Applicant: Corning Medical & Scientific
Product code: Code CCN
Device class: Class 1
Regulation: 21 CFR 868.2300
Advisory panel: Anesthesiology
Date received: 1980-08-22
Decision date: 1980-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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