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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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166 records meeting your search criteria returned- Product Code: BTM Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
VENTLAB LLC. AIRFLOW 11/28/2017
VENTLAB LLC. AIRFLOW 11/21/2017
VENTLAB LLC. AIRFLOW 11/15/2017
VENTLAB LLC. AIRFLOW 11/14/2017
VENTLAB LLC. VENTLAB 11/09/2017
VENTLAB LLC. AIRFLOW 11/02/2017
VENTLAB MEDLINE 10/30/2017
AMBU A/S SPUR® II INFANT RESUSCITATORSINGLE PATIE 10/04/2017
VENTLAB STAT CHECK 09/27/2017
VENTLAB AIRFLOW 08/28/2017
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