• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: MJN Product Problem: Difficult to Remove Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PRYTIME MEDIAL DEVICES, INC. PREBOA-PRO CATHETER 03/29/2024
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 01/11/2024
PRYTIME MEDIAL DEVICES, INC. PREBOA-PRO CATHETER 12/13/2023
PRYTIME MEDIAL DEVICES, INC. PREBOA-PRO CATHETER 11/07/2023
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 11/06/2023
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 11/02/2023
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 09/02/2023
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 08/23/2023
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 07/13/2023
PRYTIME MEDICAL DEVICES, INC. PREBOA-PRO CATHETER 07/06/2023
-
-