Digirex Digital Dental Radiography System

FDA 510(k) K060640 · Dentamerica

Substantially Equivalent

510(k) numberK060640

Submission

Device name
Digirex Digital Dental Radiography System
Applicant
Dentamerica
Industry, CA, US
Received
March 10, 2006
Decision date
April 24, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EHD – Unit, X-Ray, Extraoral With Timer
Device class
Class II (moderate risk)
Regulation
21 CFR 872.1800
Specialty
Dental

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Questions and answers

When was Digirex Digital Dental Radiography System cleared by the FDA?

Digirex Digital Dental Radiography System (K060640) received a 510(k) decision of Substantially Equivalent on April 24, 2006, 45 days after the submission was received.

What is the product code of K060640?

The FDA product code is EHD – Unit, X-Ray, Extraoral With Timer, a Class II (moderate risk) device regulated under 21 CFR 872.1800.