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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

REMSTAR PLUS CPAP SYSTEM

Manufacturer

RESPIRONICS, INC.

Date Cleared

2001-03-29

(59 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K012554,K012633,K020777,K042945,K050990,K091112,K102625,K122769

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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