INTRAORAL CAMERA ME-15— 510(k) K020206

Name: FDA 510(k) clearance K020206
Creator: U.S. Food and Drug Administration
Published: 2002-04-11

Substantially Equivalent

Dent Corp. Research & Development

FDA 510(k) clearance K020206 for INTRAORAL CAMERA ME-15, Substantially Equivalent on 2002-04-11. Applicant: Dent Corp. Research & Development. Device class: 1.

Clearance details

Applicant: Dent Corp. Research & Development
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2002-01-22
Decision date: 2002-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: White Plains, NY, US

Download summary PDF View on FDA.gov ↗

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