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TEST UROBILINOGEN IN URINE & LEUKOCYTES IN URINE

K852611 Class I Traditional
Decision Date
1985-09-03
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K852611
Product Code CDM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1785
Decision Date 1985-09-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEST UROBILINOGEN IN URINE & LEUKOCYTES IN URINE received FDA 510(k) clearance under submission number K852611, 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 1985-09-03.

Classification & Regulation

This clearance is catalogued under FDA product code CDM and 21 CFR 862.1785, within the Clinical Chemistry review panel as a Class I device.