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CLINI-TEK AUTO 2000 REFLECTANCE SPECTR

K841041 Class I Traditional
Decision Date
1984-08-24
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K841041
Product Code KQO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2900
Decision Date 1984-08-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLINI-TEK AUTO 2000 REFLECTANCE SPECTR received FDA 510(k) clearance under submission number K841041, sponsored by Miles Laboratories, Inc.. 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 1984-08-24.

Classification & Regulation

This clearance is catalogued under FDA product code KQO and 21 CFR 862.2900, within the Clinical Chemistry review panel as a Class I device.