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QM300 KAPPA LIGHT CHAINS ANTIBODY PACK

K875164 Class II Traditional
Decision Date
1988-01-22
Sponsor / Applicant
Kallestad Diag, A Div. of Erbamont, Inc.

Technical Specification

510(k) Submission ID K875164
Product Code DFH
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5550
Decision Date 1988-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QM300 KAPPA LIGHT CHAINS ANTIBODY PACK received FDA 510(k) clearance under submission number K875164, sponsored by Kallestad Diag, A Div. of Erbamont, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1988-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code DFH and 21 CFR 866.5550, within the Immunology review panel as a Class II device.