IMMUNOPLATE III RADIO IMMUNODIFFUSION— 510(k) K770548

Name: FDA 510(k) clearance K770548
Creator: U.S. Food and Drug Administration
Published: 1977-04-15

Substantially Equivalent

Hyland Therapeutic Div., Travenol Laboratories

FDA 510(k) clearance K770548 for IMMUNOPLATE III RADIO IMMUNODIFFUSION, Substantially Equivalent on 1977-04-15. Applicant: Hyland Therapeutic Div., Travenol Laboratories. Device class: 1.

Clearance details

Applicant: Hyland Therapeutic Div., Travenol Laboratories
Product code: Code JZQ
Device class: Class 1
Regulation: 21 CFR 866.4800
Advisory panel: Immunology
Date received: 1977-03-21
Decision date: 1977-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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