APIXIA DIGIREX DIGITAL DENTAL REDIOGRAPHY SYSTEM— 510(k) K120106

Name: FDA 510(k) clearance K120106
Creator: U.S. Food and Drug Administration
Published: 2012-05-07

Substantially Equivalent

Apixia, Inc.

FDA 510(k) clearance K120106 for APIXIA DIGIREX DIGITAL DENTAL REDIOGRAPHY SYSTEM, Substantially Equivalent on 2012-05-07. Applicant: Apixia, Inc.. Device class: 2.

Clearance details

Applicant: Apixia, Inc.
Product code: Product code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2012-01-13
Decision date: 2012-05-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Industry, CA, US

Download summary PDF View on FDA.gov ↗

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