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BILIRUBIN-SL (TOTAL) ASSAY, MODEL 284-10/30

K023330 Class II Traditional
Decision Date
2002-12-11
Sponsor / Applicant
Diagnostic Chemicals , Ltd.

Technical Specification

510(k) Submission ID K023330
Product Code CIG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1110
Decision Date 2002-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BILIRUBIN-SL (TOTAL) ASSAY, MODEL 284-10/30 received FDA 510(k) clearance under submission number K023330, sponsored by Diagnostic Chemicals , Ltd.. 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 2002-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code CIG and 21 CFR 862.1110, within the Clinical Chemistry review panel as a Class II device.