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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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2 records meeting your search criteria returned- Product Code: LDF Product Problem: Entrapment of Device Report Date From: 01/1/2014
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ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC WEBSTER¿ ELECTROPHYSIOLOGY CATHETER 12/21/2018
BIOSENSE WEBSTER INC FIX,5F,4P,D,5MM,10PN-DR,110 11/30/2017
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