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1,25-DIHYDROXYVITAMIN D125I RIA

K014030 Class II Traditional
Decision Date
2002-03-26
Sponsor / Applicant
DiaSorin, Inc.

Technical Specification

510(k) Submission ID K014030
Product Code MRG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1825
Decision Date 2002-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1,25-DIHYDROXYVITAMIN D125I RIA received FDA 510(k) clearance under submission number K014030, sponsored by DiaSorin, Inc.. 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 2002-03-26.

Classification & Regulation

This clearance is catalogued under FDA product code MRG and 21 CFR 862.1825, within the Clinical Chemistry review panel as a Class II device.