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CLINI-TEK SEMI-AUTOMATED URINALYSIS SYST

K821738 Class I Traditional
Decision Date
1982-07-06
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K821738
Product Code KQO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2900
Decision Date 1982-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLINI-TEK SEMI-AUTOMATED URINALYSIS SYST received FDA 510(k) clearance under submission number K821738, 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 1982-07-06.

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.