RUBELLA BIO-BEAD TITRATION KIT— 510(k) K800789

Name: FDA 510(k) clearance K800789
Creator: U.S. Food and Drug Administration
Published: 1980-06-30

Substantially Equivalent

Litton Bionetics

FDA 510(k) clearance K800789 for RUBELLA BIO-BEAD TITRATION KIT, Substantially Equivalent on 1980-06-30. Applicant: Litton Bionetics. Device class: 2.

Clearance details

Applicant: Litton Bionetics
Product code: Code GOL
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1980-04-08
Decision date: 1980-06-30
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.