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ATAC PAK BUN REAGENT

K021385 Class II Traditional
Decision Date
2002-07-12
Sponsor / Applicant
Elan Diagnostics

Technical Specification

510(k) Submission ID K021385
Product Code CDQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 2002-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ATAC PAK BUN REAGENT received FDA 510(k) clearance under submission number K021385, sponsored by Elan Diagnostics. 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 2002-07-12.

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.