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510(k) Data Aggregation

K Number

Device Name

DURASIL (MODIFICATION)

Manufacturer

THE S. F. GROUP, INC.

Date Cleared

1996-09-03

(175 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

THE S. F. GROUP, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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