ANTI NDNA IMMUNOFLOURESCENT TEST SYS— 510(k) K810981

Name: FDA 510(k) clearance K810981
Creator: U.S. Food and Drug Administration
Published: 1981-04-29

Substantially Equivalent

Immuno-Products Industries

FDA 510(k) clearance K810981 for ANTI NDNA IMMUNOFLOURESCENT TEST SYS, Substantially Equivalent on 1981-04-29. Applicant: Immuno-Products Industries. Device class: 2.

Clearance details

Applicant: Immuno-Products Industries
Product code: Code DHC
Device class: Class 2
Regulation: 21 CFR 866.5820
Advisory panel: Immunology
Date received: 1981-04-13
Decision date: 1981-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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