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510(k) Data Aggregation

K Number

Device Name

9000 SERIES FILTER & FILTER/HME

Manufacturer

ENTERNET MEDICAL, INC.

Date Cleared

1997-02-21

(199 days)

Product Code

Regulation Number

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Applicant Name (Manufacturer) :

ENTERNET MEDICAL, INC.

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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