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510(k) Data Aggregation

K Number

Device Name

PATIENT EXAMINATION GLOVE (POWDERED)

Manufacturer

MEDLINE PRODUCTS CO. LTD.

Date Cleared

1996-07-26

(316 days)

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Regulation Number

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Applicant Name (Manufacturer) :

MEDLINE PRODUCTS CO. LTD.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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