VOLU-SOL TAP WATER SUBSTITUTE— 510(k) K822037

Name: FDA 510(k) clearance K822037
Creator: U.S. Food and Drug Administration
Published: 1982-08-03

Substantially Equivalent

Volu Sol Medical Industries

FDA 510(k) clearance K822037 for VOLU-SOL TAP WATER SUBSTITUTE, Substantially Equivalent on 1982-08-03. Applicant: Volu Sol Medical Industries. Device class: 1.

Clearance details

Applicant: Volu Sol Medical Industries
Product code: Code PPM
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1982-07-12
Decision date: 1982-08-03
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.