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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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403 records meeting your search criteria returned- Product Code: LNQ Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 06/19/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/17/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/10/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/09/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/07/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/02/2018
MEDTRONIC NEUROMODULATION INTESTINAL STIMULATOR 04/19/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 04/06/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 04/04/2018
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ENTERRA 04/01/2018
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