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510(k) Data Aggregation

K Number

Device Name

COMOACT ULTRASONIC NEBULIZER, MODEL 3060

Manufacturer

Date Cleared

2001-06-14

(302 days)

Product Code

Regulation Number

Type

Panel

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N/A

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Device Name :

COMOACT ULTRASONIC NEBULIZER, MODEL 3060

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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