ABNORMAL GLYCOSYLATED HEMOGLOBIN CONTROL— 510(k) K811000

Name: FDA 510(k) clearance K811000
Creator: U.S. Food and Drug Administration
Published: 1981-05-08

Substantially Equivalent

Corning Medical & Scientific

FDA 510(k) clearance K811000 for ABNORMAL GLYCOSYLATED HEMOGLOBIN CONTROL, Substantially Equivalent on 1981-05-08. Applicant: Corning Medical & Scientific. Device class: 2.

Clearance details

Applicant: Corning Medical & Scientific
Product code: Code LCP
Device class: Class 2
Regulation: 21 CFR 864.7470
Advisory panel: Hematology
Date received: 1981-04-13
Decision date: 1981-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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