meddevicedb.com FDA Device Reference

MAGIC NO BOIL B12/FOLATE RADIOIMMUNOASSAY

K854945 Class II Traditional
Decision Date
1986-02-11
Sponsor / Applicant
Ciba Corning Diagnostics Corp.

Technical Specification

510(k) Submission ID K854945
Product Code CDD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1810
Decision Date 1986-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAGIC NO BOIL B12/FOLATE RADIOIMMUNOASSAY received FDA 510(k) clearance under submission number K854945, sponsored by Ciba Corning Diagnostics Corp.. 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 1986-02-11.

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.