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510(k) Data Aggregation

K Number

Device Name

SUTURE APPLICATOR

Manufacturer

LAURUS MEDICAL GROUP

Date Cleared

1997-02-07

(78 days)

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Regulation Number

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Applicant Name (Manufacturer) :

LAURUS MEDICAL GROUP

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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