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ABNORMAL GLYCOSYLATED HEMOGLOBIN CONTROL

K811000 Class II Traditional
Decision Date
1981-05-08
Sponsor / Applicant
Corning Medical & Scientific

Technical Specification

510(k) Submission ID K811000
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 1981-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ABNORMAL GLYCOSYLATED HEMOGLOBIN CONTROL received FDA 510(k) clearance under submission number K811000, sponsored by Corning Medical & Scientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1981-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.