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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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413 records meeting your search criteria returned- Product Code: DTK Product Problem: Entrapment of Device Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
ARGON MEDICAL DEVICES, INC. OPTION ELITE RETRIEVABLE VENA CAVA FILTE 08/25/2021
ARGON MEDICAL DEVICES OPTION RETRIEVABLE VENA CAVA FILTER 08/11/2021
ARGON MEDICAL DEVICES, INC. OPTION IVC FILTER 07/29/2021
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 07/08/2021
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 06/16/2021
BARD PERIPHERAL VASCULAR, INC. RECOVERY 06/04/2021
ARGON MEDICAL DEVICES OPTION VENA CAVA FILTER 06/03/2021
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 06/03/2021
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 06/03/2021
ARGON MEDICAL DEVICES OPTION ELITE RETRIEVABLE VENA CAVA FILTE 06/03/2021
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