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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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135 records meeting your search criteria returned- Product Code: DRB Patient Problem: Pericardial Effusion Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 08/14/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 06/24/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 06/24/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 03/04/2019
THE SPECTRANETICS CORPORATION SEPCTRANETICS LEAD LOCKING DEVICE 12/12/2018
THE SPECTRANETICS CORPORATION SPECTRANETICS LLD EZ LEAD LOCKING DEVICE 06/13/2018
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 08/18/2017
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 07/21/2017
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 07/21/2017
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 05/01/2017
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