• 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 
 > 
 
36 records meeting your search criteria returned- Product Code: PEP Product Problem: False Negative Result Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PROGENIKA BIOPHARMA, S.A ID CORE XT 02/29/2024
PROGENIKA BIOPHARMA, S.A ID CORE XT 02/29/2024
PROGENIKA BIOPHARMA, S.A ID CORE XT 02/29/2024
PROGENIKA BIOPHARMA, S.A ID CORE XT 02/29/2024
PROGENIKA BIOPHARMA, S.A ID CORE XT 02/15/2024
PROGENIKA BIOPHARMA, S.A ID CORE XT 10/02/2023
BIOARRAY SOLUTIONS, LIMITED PRECISETYPE HEA MOLECULAR BEADCHIP TEST 08/01/2023
PROGENIKA BIOPHARMA, S.A ID CORE XT 07/06/2023
PROGENIKA BIOPHARMA, S.A ID CORE XT 06/28/2023
PROGENIKA BIOPHARMA, S.A ID CORE XT 06/09/2023
-
-