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J.T. BAKER CERULOPLASMIN NEPHELOMETRIC

K801661 Class II Traditional
Decision Date
1980-09-16
Sponsor / Applicant
J.T. Baker Chemical Co.

Technical Specification

510(k) Submission ID K801661
Product Code DDB
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5210
Decision Date 1980-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

J.T. BAKER CERULOPLASMIN NEPHELOMETRIC received FDA 510(k) clearance under submission number K801661, sponsored by J.T. Baker Chemical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1980-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code DDB and 21 CFR 866.5210, within the Immunology review panel as a Class II device.