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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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13 records meeting your search criteria returned- Product Code: DRX Patient Problem: Lead(s), Burn(s) From Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
NEOTECH PRODUCTS LLC NEOTECH PRODUCTS LLC 05/24/2018
NEOTECH PRODUCTS LLC NEOTECH PRODUCTS LLC 05/24/2018
NEOTECH PRODUCTS LLC NEOTECH PRODUCTS LLC 05/23/2018
NEOTECH PRODUCTS LLC NEOTECH PRODUCTS LLC 05/23/2018
BIO PROTECH INC ELECTRODE, ECG, PREWIRED, NEONATAL, CLOT 09/06/2017
NEOTECH PRODUCTS NEOTECH 03/13/2017
NEOTECH NEOTECH 01/26/2017
NEOTECH NEOTECH 12/06/2016
NEOTECH NEOTECH 11/10/2016
NEOTECH NEOTECH 11/10/2016
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