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ARCHITECT TOTAL BILIRUBIN

K121985 Class II Traditional
Decision Date
2013-02-01
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K121985
Product Code CIG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1110
Decision Date 2013-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARCHITECT TOTAL BILIRUBIN received FDA 510(k) clearance under submission number K121985, sponsored by Abbott 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 2013-02-01.

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.