EIA RUBELLA— 510(k) K812787

Substantially Equivalent

Gilford

FDA 510(k) clearance K812787 for EIA RUBELLA, Substantially Equivalent on 1981-11-27. Applicant: Gilford. Device class: 2.

Clearance details

Applicant: Gilford
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1981-10-05
Decision date: 1981-11-27
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.