LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT— 510(k) K802661

Name: FDA 510(k) clearance K802661
Creator: U.S. Food and Drug Administration
Published: 1980-12-10

Substantially Equivalent

Damon Corp.

FDA 510(k) clearance K802661 for LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT, Substantially Equivalent on 1980-12-10. Applicant: Damon Corp.. Device class: 1.

Clearance details

Applicant: Damon Corp.
Product code: Code CDZ
Device class: Class 1
Regulation: 21 CFR 862.1680
Advisory panel: Clinical Chemistry
Date received: 1980-10-28
Decision date: 1980-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.