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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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161 records meeting your search criteria returned- Product Code: MLV Product Problem: Unintended Movement Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 02/09/2017
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 01/31/2017
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 01/30/2017
AGA MEDICAL CORPORATION AMPLATZER PFO OCCLUDER 01/17/2017
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 01/12/2017
AGA MEDICAL CORPORATION AMPLATZER CRIBRIFORM OCCLUDER 01/10/2017
AGA MEDICAL CORPORATION AMPLATZER MUSCULAR VSD OCCLUDER 01/04/2017
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 12/22/2016
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 12/08/2016
AGA MEDICAL CORPORATION AMPLATZER SEPTAL OCCLUDER 12/07/2016
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