meddevicedb.com FDA Device Reference

Elecsys Vitamin B12 II assay, Elecsys Vitamin B12 II CalSet

K151786 Class II Traditional
Decision Date
2015-09-24
Sponsor / Applicant
Roche Diagnostics

Technical Specification

510(k) Submission ID K151786
Product Code CDD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1810
Decision Date 2015-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Elecsys Vitamin B12 II assay, Elecsys Vitamin B12 II CalSet received FDA 510(k) clearance under submission number K151786, sponsored by Roche 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 2015-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code CDD and 21 CFR 862.1810, within the Clinical Chemistry review panel as a Class II device.