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

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 
 3 
 4 
 > 
 
33 records meeting your search criteria returned- Product Code: KMW Product Problem: Nonstandard Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NAKANISHI INC. NSK 05/11/2022
NAKANISHI INC. NSK 04/17/2022
NAKANISHI INC. NSK 04/07/2022
NAKANISHI INC. NSK 04/07/2022
NAKANISHI INC. NSK 03/07/2022
NAKANISHI INC. NSK 01/14/2022
NAKANISHI INC. NSK 12/22/2021
NAKANISHI INC. NSK 12/15/2021
NAKANISHI INC. NSK 10/21/2021
NAKANISHI INC. NSK 10/20/2021
-
-