CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT)— 510(k) K011147

Name: FDA 510(k) clearance K011147
Creator: U.S. Food and Drug Administration
Published: 2002-02-15

Substantially Equivalent

Cavitat Medical Technologies, Inc.

FDA 510(k) clearance K011147 for CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT), Substantially Equivalent on 2002-02-15. Applicant: Cavitat Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Cavitat Medical Technologies, Inc.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2001-04-16
Decision date: 2002-02-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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