ELVI-AMINOLEVULINIC ACID— 510(k) K792407

Name: FDA 510(k) clearance K792407
Creator: U.S. Food and Drug Administration
Published: 1980-01-16

Substantially Equivalent

Volu Sol Medical Industries

FDA 510(k) clearance K792407 for ELVI-AMINOLEVULINIC ACID, Substantially Equivalent on 1980-01-16. Applicant: Volu Sol Medical Industries. Device class: 2.

Clearance details

Applicant: Volu Sol Medical Industries
Product code: Code DIJ
Device class: Class 2
Regulation: 21 CFR 862.3550
Advisory panel: Clinical Toxicology
Date received: 1979-11-26
Decision date: 1980-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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