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NO-BOIL VITABIN B12 5760 FOLATE 125I

K813183 Class II Traditional
Decision Date
1982-03-05
Sponsor / Applicant
Corning Medical & Scientific

Technical Specification

510(k) Submission ID K813183
Product Code CDD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1810
Decision Date 1982-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NO-BOIL VITABIN B12 5760 FOLATE 125I received FDA 510(k) clearance under submission number K813183, sponsored by Corning Medical & Scientific. 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 1982-03-05.

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.