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DIAZYME LIQUID STABLE ENZYMATIC SODIUM ASSAY, MODEL DZ114B

K082763 Class II Special
Decision Date
2008-11-12
Sponsor / Applicant
Diazyme Laboratories

Technical Specification

510(k) Submission ID K082763
Product Code MZU
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1665
Decision Date 2008-11-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAZYME LIQUID STABLE ENZYMATIC SODIUM ASSAY, MODEL DZ114B received FDA 510(k) clearance under submission number K082763, sponsored by Diazyme Laboratories. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2008-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code MZU and 21 CFR 862.1665, within the Clinical Chemistry review panel as a Class II device.