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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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461 records meeting your search criteria returned- Product Code: LKK Product Problem: Inappropriate or Unexpected Reset Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/28/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/31/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 12/02/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 11/17/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 11/01/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/28/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 08/26/2021
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 08/18/2021
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 08/06/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 07/02/2021
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