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DIAZYME LIQUID STABLE ENZYMATIC POTASSIUM ASSAY KIT, MODEL DZ113C-X, DIAZYME LIQUID STABLE ENZYMATIC POTASSIUM ASSAY CAL

K091455 Class II Traditional
Decision Date
2009-08-14
Sponsor / Applicant
Diazyme Laboratories

Technical Specification

510(k) Submission ID K091455
Product Code MZV
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 2009-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAZYME LIQUID STABLE ENZYMATIC POTASSIUM ASSAY KIT, MODEL DZ113C-X, DIAZYME LIQUID STABLE ENZYMATIC POTASSIUM ASSAY CAL received FDA 510(k) clearance under submission number K091455, sponsored by Diazyme Laboratories. 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 2009-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code MZV and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.