meddevicedb.com FDA Device Reference

LAS-R BETA LIPOPROTEIN TEST

K771912 Class II Traditional
Decision Date
1977-10-19
Sponsor / Applicant
Hyland Therapeutic Div., Travenol Laboratories

Technical Specification

510(k) Submission ID K771912
Product Code DFC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5600
Decision Date 1977-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAS-R BETA LIPOPROTEIN TEST received FDA 510(k) clearance under submission number K771912, sponsored by Hyland Therapeutic Div., Travenol Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1977-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code DFC and 21 CFR 866.5600, within the Immunology review panel as a Class II device.