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510(k) Data Aggregation

K Number

Device Name

OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE)

Manufacturer

Date Cleared

2001-02-05

(66 days)

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Regulation Number

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Applicant Name (Manufacturer) :

OPTOVENT AB

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty

Intended Use

Device Description

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