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510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

RESPIEVENTS, VERSION 4.2

Manufacturer

NON-INVASIVE MONITORING SYSTEMS, INC.

Date Cleared

2000-07-26

(86 days)

Product Code

Regulation Number

Type

Panel

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

K011903,K012020

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

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