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510(k) Data Aggregation

K Number

Device Name

SIDEPORT PINCH CLAMP DEVICE

Manufacturer

MEDIVICE SYSTEMS, LTD.

Date Cleared

2001-06-27

(96 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

MEDIVICE SYSTEMS, LTD.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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