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ALBUMIN NEPHELOMETRIC ASSAY

K801362 Class I Traditional
Decision Date
1980-07-21
Sponsor / Applicant
J.T. Baker Chemical Co.

Technical Specification

510(k) Submission ID K801362
Product Code JQX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2700
Decision Date 1980-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALBUMIN NEPHELOMETRIC ASSAY received FDA 510(k) clearance under submission number K801362, sponsored by J.T. Baker Chemical Co.. 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 1980-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code JQX and 21 CFR 862.2700, within the Clinical Chemistry review panel as a Class I device.