LAS-R HUMAN HAPTOGLOBIN TEST— 510(k) K760917

Name: FDA 510(k) clearance K760917
Creator: U.S. Food and Drug Administration
Published: 1976-12-30

Substantially Equivalent

Hyland Therapeutic Div., Travenol Laboratories

FDA 510(k) clearance K760917 for LAS-R HUMAN HAPTOGLOBIN TEST, Substantially Equivalent on 1976-12-30. Applicant: Hyland Therapeutic Div., Travenol Laboratories. Device class: 2.

Clearance details

Applicant: Hyland Therapeutic Div., Travenol Laboratories
Product code: Code DFT
Device class: Class 2
Regulation: 21 CFR 866.5550
Advisory panel: Immunology
Date received: 1976-10-28
Decision date: 1976-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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