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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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138 records meeting your search criteria returned- Product Code: NKE Product Problem: Failure to Interrogate Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. PERCEPTA CRT-P MRI SURESCAN 06/13/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ALLURE MP RF CRT-P 04/16/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUADRA ALLURE MP RF CRT-P 04/10/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUADRA ALLURE MP CRT-P 03/29/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. PERCEPTA QUAD CRTP 03/15/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SOLARA QUAD CRTP 03/01/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FRONTIER II 12/20/2018
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) QUADRA ALLURE MP RF CRT-P 12/19/2018
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) FRONTIER II 12/12/2018
MEDTRONIC EUROPE SARL SOLARA QUAD CRTP 11/01/2018
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