JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002— 510(k) K020070

Name: FDA 510(k) clearance K020070
Creator: U.S. Food and Drug Administration
Published: 2002-02-01

Substantially Equivalent

Progeny, Inc.

FDA 510(k) clearance K020070 for JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002, Substantially Equivalent on 2002-02-01. Applicant: Progeny, Inc.. Device class: 2.

Clearance details

Applicant: Progeny, Inc.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2002-01-09
Decision date: 2002-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo Grove, IL, US

Download summary PDF View on FDA.gov ↗

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