710 FLUOROMETER/DENSITOMETER— 510(k) K810619

Name: FDA 510(k) clearance K810619
Creator: U.S. Food and Drug Administration
Published: 1981-03-27

Substantially Equivalent

Corning Medical & Scientific

FDA 510(k) clearance K810619 for 710 FLUOROMETER/DENSITOMETER, Substantially Equivalent on 1981-03-27. Applicant: Corning Medical & Scientific. Device class: 1.

Clearance details

Applicant: Corning Medical & Scientific
Product code: Code JQT
Device class: Class 1
Regulation: 21 CFR 862.2400
Advisory panel: Clinical Chemistry
Date received: 1981-03-09
Decision date: 1981-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MA, US

Download summary PDF View on FDA.gov ↗

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