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510(k) Data Aggregation

K Number

Device Name

DUOSTAR

Manufacturer

MTI CORP./ ELECTROSTAR S.A.-HAITI

Date Cleared

1998-09-30

(329 days)

Product Code

Regulation Number

Why did this record match?

Applicant Name (Manufacturer) :

MTI CORP./ ELECTROSTAR S.A.-HAITI

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

PHYSICIANS ONLY BY SALE AND USE FOR CAUTERIZING AND CUTTING FOR SURGICAL PROGEDURES

Device Description

Not Found

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