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510(k) Data Aggregation

K Number

Device Name

NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE

Manufacturer

PHOENIX MEDICAL TECHNOLOGY, INC.

Date Cleared

2000-04-14

(81 days)

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Regulation Number

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Applicant Name (Manufacturer) :

PHOENIX MEDICAL TECHNOLOGY, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

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