• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: JCX Product Problem: Device Contamination with Body Fluid Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. PUMP MAX CANISTER 12/03/2019
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 06/06/2019
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 12/07/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110V 10/18/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110V 10/04/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110V 08/27/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 06/01/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 220V 04/26/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 04/09/2018
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 03/13/2018
-
-