Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
  • 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 
 3 
 
 
21 records meeting your search criteria returned- Product Code: NJK Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 11/21/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 08/07/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 07/25/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL VALVE (EBV) 07/24/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 04/17/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 02/27/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 02/20/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 01/02/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 01/02/2019
PULMONX CORPORATION ZEPHYR ENDOBRONCHIAL DELIVERY CATHETER 12/20/2018
-
-