VIVID, MODELS 40-A0001, 40-A0004, 40-A0006— 510(k) K090079

Name: FDA 510(k) clearance K090079
Creator: U.S. Food and Drug Administration
Published: 2009-05-01

Substantially Equivalent

Progeny, Inc.

FDA 510(k) clearance K090079 for VIVID, MODELS 40-A0001, 40-A0004, 40-A0006, Substantially Equivalent on 2009-05-01. Applicant: Progeny, Inc.. Device class: 1.

Clearance details

Applicant: Progeny, Inc.
Product code: Code EIA
Device class: Class 1
Regulation: 21 CFR 872.6640
Advisory panel: Dental
Date received: 2009-01-12
Decision date: 2009-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lincolnshire, IL, US

Download summary PDF View on FDA.gov ↗

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