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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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277 records meeting your search criteria returned- Product Code: LIT Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 03/04/2024
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 02/22/2024
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 02/05/2024
ABBOTT VASCULAR ARMADA 18 PTA CATHETER 01/10/2024
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 11/06/2023
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 10/30/2023
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 10/30/2023
ABBOTT VASCULAR RX VIATRAC 14 PLUS PERIPHERAL DILATATION 10/19/2023
ABBOTT VASCULAR ARMADA 18 PTA CATHETER 10/09/2023
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 09/18/2023
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