• 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
153 records meeting your search criteria returned- Product Code: MHX Product Problem: Appropriate Term/Code Not Available Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 12/16/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 12/15/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 12/13/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 12/08/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 12/02/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 11/22/2022
REMOTE DIAGNOSTIC TECHNOLOGIES (RDT) TEMPUS PRO 11/09/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 11/08/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 11/08/2022
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO 11/08/2022
-
-