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ENZYMATIC UREA NITROGEN REAGENT SET REVI

K800719 Class II Traditional
Decision Date
1980-05-08
Sponsor / Applicant
Macomb Chemical Co.

Technical Specification

510(k) Submission ID K800719
Product Code CDQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 1980-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENZYMATIC UREA NITROGEN REAGENT SET REVI received FDA 510(k) clearance under submission number K800719, sponsored by Macomb 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 1980-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code CDQ and 21 CFR 862.1770, within the Clinical Chemistry review panel as a Class II device.