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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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4 records meeting your search criteria returned- Product Code: ITI Patient Problem: Vertigo Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SUNRISE MEDICAL (US) LLC QUICKIE Q500M 05/08/2023
ALBER GMBH E-MOTION M25 03/02/2023
PRIDE MOBILITY PRODUCTS PRIDE MOBILITY PRODUCTS 06/25/2018
INVACARE TAYLOR STREET POWERED WHEELCHAIR 05/30/2014
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