PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).— 510(k) K070664

Name: FDA 510(k) clearance K070664
Creator: U.S. Food and Drug Administration
Published: 2007-04-26

Substantially Equivalent

Progeny, Inc.

FDA 510(k) clearance K070664 for PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8)., Substantially Equivalent on 2007-04-26. Applicant: Progeny, Inc.. Device class: 2.

Clearance details

Applicant: Progeny, Inc.
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2007-03-09
Decision date: 2007-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buffalo Grove, IL, US

Download summary PDF View on FDA.gov ↗

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