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510(k) Data Aggregation

K Number

Device Name

CAVITAT ULTRASOUND BONE DENSITOMETER (CAVITAT)

Manufacturer

CAVITAT MEDICAL TECHNOLOGIES, INC.

Date Cleared

2002-02-15

(305 days)

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Regulation Number

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Applicant Name (Manufacturer) :

CAVITAT MEDICAL TECHNOLOGIES, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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