GLYCOPROTEIN TEST, LAS-R HUMAN 1-ACID— 510(k) K771879

Name: FDA 510(k) clearance K771879
Creator: U.S. Food and Drug Administration
Published: 1977-10-19

Substantially Equivalent

Hyland Therapeutic Div., Travenol Laboratories

FDA 510(k) clearance K771879 for GLYCOPROTEIN TEST, LAS-R HUMAN 1-ACID, Substantially Equivalent on 1977-10-19. Applicant: Hyland Therapeutic Div., Travenol Laboratories. Device class: 1.

Clearance details

Applicant: Hyland Therapeutic Div., Travenol Laboratories
Product code: Code DEN
Device class: Class 1
Regulation: 21 CFR 866.5420
Advisory panel: Immunology
Date received: 1977-10-04
Decision date: 1977-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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