CD-DENT DIGITAL IMAGING DEVICES FOR DENTAL X-RAY SYSTEMS, MODELS 600, 1000 AND 2000— 510(k) K990049

Name: FDA 510(k) clearance K990049
Creator: U.S. Food and Drug Administration
Published: 1999-03-12

Substantially Equivalent

Digident , Ltd.

FDA 510(k) clearance K990049 for CD-DENT DIGITAL IMAGING DEVICES FOR DENTAL X-RAY SYSTEMS, MODELS 600, 1000 AND 2000, Substantially Equivalent on 1999-03-12. Applicant: Digident , Ltd.. Device class: 2.

Clearance details

Applicant: Digident , Ltd.
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 1999-01-07
Decision date: 1999-03-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

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