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GLYCOPROTEIN TEST, LAS-R HUMAN 1-ACID

K771879 Class I Traditional
Decision Date
1977-10-19
Sponsor / Applicant
Hyland Therapeutic Div., Travenol Laboratories

Technical Specification

510(k) Submission ID K771879
Product Code DEN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5420
Decision Date 1977-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLYCOPROTEIN TEST, LAS-R HUMAN 1-ACID received FDA 510(k) clearance under submission number K771879, 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 DEN and 21 CFR 866.5420, within the Immunology review panel as a Class I device.