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TOTAL BILE ACIDS ASSAY, MODEL DZ042A

K051714 Class II Traditional
Decision Date
2005-12-07
Sponsor / Applicant
Diazyme Laboratories

Technical Specification

510(k) Submission ID K051714
Product Code KWW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1177
Decision Date 2005-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TOTAL BILE ACIDS ASSAY, MODEL DZ042A received FDA 510(k) clearance under submission number K051714, 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 2005-12-07.

Classification & Regulation

This clearance is catalogued under FDA product code KWW and 21 CFR 862.1177, within the Clinical Chemistry review panel as a Class II device.