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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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5 records meeting your search criteria returned- Product Code: BWF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MONAGHAN MEDICAL CORP. AEROBIKA DEVICE 04/15/2020
VYAIRE MEDICAL, INC. AIRLIFE VYAIRE INCENTIVE SPIROMETER 09/03/2019
TELEFLEX MEDICAL VOLDYNE2500 VOLUMETRIC EXERCISER 07/08/2019
ACTEGY LTD AEROSURE MEDIC 05/31/2018
SMITHS MEDICAL ASD, INC. COACH 2 INCENTIVE SPIROMETER 12/05/2014
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