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

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..

Clearance details

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

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