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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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63 records meeting your search criteria returned- Product Code: JOW Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DJO, LLC AIRCAST 11/06/2017
COVIDIEN KENDALL SCD 07/21/2017
INNOVAMED HEALTH LLC AIRCAST 05/12/2017
INNOVAMED HEALTH LLC AIRCAST 03/21/2017
MEDICAL COMPRESSION SYSTEMS DBN LTD. ACTIVECARE+SFT 02/20/2017
GETINGE (SUZHOU) CO., LTD. FLOWTRON ACS 900 01/18/2017
ARJOHUNTLEIGH POLSKA SP. Z O.O. TRIPULSE GARMENT 11/25/2016
ARJOHUNTLEIGH POLSKA SP. Z O.O. TRI PULSE GARMENT 11/10/2016
GETINGE (SUZHOU) CO., LTD. FLOWTRON ACS900 08/29/2016
GETINGE (SUZHOU) CO., LTD. FLOWTRON ACS900 08/29/2016
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