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510(k) Data Aggregation

K Number

Device Name

PREPOWDERED LATEX EXAMINATION GLOVE

Manufacturer

BESGLOVE HEALTHCARE SDN. BHD.

Date Cleared

1997-03-11

(43 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

BESGLOVE HEALTHCARE SDN. BHD.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

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