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UV GLUCOSE DETERM., AUTO CHEM. ANALYZERS

K771102 Class II Traditional
Decision Date
1977-11-22
Sponsor / Applicant
The Dow Chemical Co.

Technical Specification

510(k) Submission ID K771102
Product Code LFR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1977-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UV GLUCOSE DETERM., AUTO CHEM. ANALYZERS received FDA 510(k) clearance under submission number K771102, sponsored by The Dow Chemical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1977-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code LFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.