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510(k) Data Aggregation

K Number

Device Name

SILIMED PECTORAL IMPLANT

Manufacturer

Date Cleared

2005-02-23

(208 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

SILIMED, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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