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VENTRIA APO A-1 ALPHA-1 LIPOTROTEIN

K840830 Class II Traditional
Decision Date
1984-05-21
Sponsor / Applicant
Ventrex Laboratories, Inc.

Technical Specification

510(k) Submission ID K840830
Product Code DER
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5580
Decision Date 1984-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VENTRIA APO A-1 ALPHA-1 LIPOTROTEIN received FDA 510(k) clearance under submission number K840830, sponsored by Ventrex Laboratories, 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 1984-05-21.

Classification & Regulation

This clearance is catalogued under FDA product code DER and 21 CFR 866.5580, within the Immunology review panel as a Class II device.