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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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18 records meeting your search criteria returned- Product Code: MJN Patient Problem: Insufficient Information Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
PRYTIME MEDIAL DEVICES, INC. PREBOA-PRO CATHETER 03/29/2024
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 09/28/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT WITH T-PORT (INL 09/19/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 04/20/2023
MICRO THERAPEUTICS, INC. DBA EV3 HYPERFORM 02/04/2023
BALT USA ECLIPSE2L BALLOON CATHETER 06/14/2022
Unknown Manufacturer OCCLUSION BALLOON CATHETER 08/30/2021
LUCAS MEDICAL INC LMI CAROTID ENDARTERECTOMY SHUNT CATHETE 08/23/2021
BALT USA ECLIPSE2L BALLOON CATHETER 08/20/2021
SPECTRANETICS CORPORATION BRIDGE OCCLUSION BALLOON 06/30/2021
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