• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 > 
 
19 records meeting your search criteria returned- Product Code: NIM Product Problem: Crack Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CORDIS US CORP. PRECISE PRO RX OUS 02/06/2024
CORDIS US. CORP PRECISE PRO RX 01/16/2024
CORDIS US CORP. PRECISE PRO RX 06/09/2023
CORDIS CORPORATION PRECISE PRO RX US CAROTID SYST 08/20/2020
CORDIS CORPORATION PRECISE PRO RX 8X40 01/17/2019
CORDIS CORPORATION PRECISE PRO RX US CAROTID SYST 05/18/2018
CORDIS CORPORATION PRECISE PRO RX 8X40 04/24/2018
CORDIS CORPORATION PRECISE PRO RX 9X40 02/13/2018
CORDIS CORPORATION PRECISE PRO RX US CAROTID SYST 12/01/2017
AV-TEMECULA-CT RX ACCULINK CAROTID STENT SYSTEM 10/26/2017
-
-