UNIPORT SELF-CONTAINED PORTABLE DENTAL UNIT— 510(k) K040117

Name: FDA 510(k) clearance K040117
Creator: U.S. Food and Drug Administration
Published: 2004-04-21

Substantially Equivalent

Arrow Industries, LLC

FDA 510(k) clearance K040117 for UNIPORT SELF-CONTAINED PORTABLE DENTAL UNIT, Substantially Equivalent on 2004-04-21. Applicant: Arrow Industries, LLC. Device class: 1.

Clearance details

Applicant: Arrow Industries, LLC
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2004-01-20
Decision date: 2004-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Neche, ND, US

Download summary PDF View on FDA.gov ↗

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