meddevicedb.com FDA Device Reference

HEMOPEXIN NEPHELOMETRIC ASSAY

K801432 Class II Traditional
Decision Date
1980-07-08
Sponsor / Applicant
J.T. Baker Chemical Co.

Technical Specification

510(k) Submission ID K801432
Product Code CZX
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5490
Decision Date 1980-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOPEXIN NEPHELOMETRIC ASSAY received FDA 510(k) clearance under submission number K801432, 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 1980-07-08.

Classification & Regulation

This clearance is catalogued under FDA product code CZX and 21 CFR 866.5490, within the Immunology review panel as a Class II device.