ELVI BLOOD UREA NITROGEN— 510(k) K792417

Name: FDA 510(k) clearance K792417
Creator: U.S. Food and Drug Administration
Published: 1979-12-07

Substantially Equivalent

Volu Sol Medical Industries

FDA 510(k) clearance K792417 for ELVI BLOOD UREA NITROGEN, Substantially Equivalent on 1979-12-07. Applicant: Volu Sol Medical Industries. Device class: 2.

Clearance details

Applicant: Volu Sol Medical Industries
Product code: Code CDL
Device class: Class 2
Regulation: 21 CFR 862.1770
Advisory panel: Clinical Chemistry
Date received: 1979-11-26
Decision date: 1979-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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