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CALCIUM

K062855 Class II Traditional
Decision Date
2006-11-22
Sponsor / Applicant
Abbott Laboratories

Technical Specification

510(k) Submission ID K062855
Product Code CJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1145
Decision Date 2006-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALCIUM received FDA 510(k) clearance under submission number K062855, 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 2006-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code CJY and 21 CFR 862.1145, within the Clinical Chemistry review panel as a Class II device.