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510(k) Data Aggregation

K Number

Device Name

PORTSMART NEEDLE DE-ACCESS ENCLOSURE

Manufacturer

Date Cleared

1997-01-03

(51 days)

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Regulation Number

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Applicant Name (Manufacturer) :

JIREH, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

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