Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
 1 
 2 
 > 
 
20 records meeting your search criteria returned- Product Code: LNQ Patient Problem: Abdominal Cramps Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 10/07/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 08/13/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 01/31/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 10/30/2017
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 09/27/2017
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 02/06/2017
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ENTERRA 09/08/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 08/16/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. ENTERRA 05/17/2016
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ENTERRA 05/16/2016
-
-