• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 > 
 
73 records meeting your search criteria returned- Product Code: PUM Report Date From: 1/1/2020 Report Date To: 12/31/2020

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 03/18/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM 03/16/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 03/16/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 03/11/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 02/19/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 02/12/2020
CLARET MEDICAL, INC. SENTINEL 01/31/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 01/27/2020
CLARET MEDICAL, INC. SENTINEL CEREBRAL PROTECTION SYSTEM (US) 01/27/2020
CLARET MEDICAL, INC. SENTINEL 01/17/2020
-
-