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QUANTAPHASE II B12/FOLATE

K935286 Class II Traditional
Decision Date
1994-02-18
Sponsor / Applicant
Bio-Rad

Technical Specification

510(k) Submission ID K935286
Product Code CGN
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1295
Decision Date 1994-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUANTAPHASE II B12/FOLATE received FDA 510(k) clearance under submission number K935286, sponsored by Bio-Rad. 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 1994-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code CGN and 21 CFR 862.1295, within the Clinical Chemistry review panel as a Class II device.