• 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 
 5 
 6 
 7 
 8 
 > 
 
75 records meeting your search criteria returned- Product Code: HGI Patient Problem: Insufficient Information Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOPERSURGICAL, INC. LEEP PRECISION 11/28/2021
COOPERSURGICAL , INC. LEEP SYSTEM 1000 ESU GEN. 11/22/2021
COOPERSURGICAL , INC. LEEP SYSTEM 1000 ESU GEN. 10/14/2021
COOPERSURGICAL, INC. LEEP PRECISION GENERATOR 10/13/2021
COOPERSURGICAL, INC. LEEP SYSTEM 1000 ESU GEN 10/12/2021
COOPERSURGICAL, INC. LEEP PRECISION GENERATOR 10/12/2021
COOPERSURGICAL, INC. LEEP PRECISION GENERATOR 10/11/2021
COOPERSURGICAL, INC. LEEP PRECISION GENERATOR 10/02/2021
COOPERSURGICAL, INC. LEEP PRECISION GENERATOR 10/01/2021
COOPERSURGICAL, INC. LEEP SYSTEM 1000 ESU GEN 10/01/2021
-
-