• 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
 

 
 
10 records meeting your search criteria returned- Product Code: FCG Patient Problem: Abscess Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WILSON-COOK MEDICAL INC ECHOTIP ULTRA FIDUCIAL NEEDLE 10/31/2023
COOK IRELAND LTD ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND 05/02/2023
COVIDIEN LP BARRX UNKNOWN BEACON NEEDLE 07/20/2022
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 06/09/2022
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 08/06/2021
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U200H 12/16/2019
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-220H/230 12/16/2019
OLYMPUS MEDICAL SYSTEMS CORP. ASPIRATION NEEDLE 12/16/2019
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 12/12/2019
COOK IRELAND LTD ECHOTIP PROCORE HIGH DEFINITION ULTRASOU 09/03/2019
-
-