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

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
 

 
 
9 records meeting your search criteria returned- Product Code: FCG Product Problem: Device Slipped Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/16/2020
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/03/2020
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 06/18/2020
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 06/18/2020
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 05/20/2020
OLYMPUS RESPIRATORY AMERICA SINGLE USE ASPIRATION NEEDLE 10/27/2017
OLYMPUS MEDICAL SYSTEMS CORPORATION VIZISHOT ENDOBRONCHIAL ULTRASOUND ASPIRA 05/19/2015
COOK, INC. ECHOTIP ULTRA 10/28/2014
COOK, INC. PENTEX BRONCHOSCOPE EBUS 10/28/2014
-
-