• 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 
 
 
11 records meeting your search criteria returned- Product Code: KTI Patient Problem: Insufficient Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GYRUS ACMI, INC. SINGLE USE ASPIRATION NEEDLE 11/04/2023
GYRUS ACMI, INC. SINGLE USE ASPIRATION NEEDLE 11/03/2023
GYRUS ACMI, INC. SINGLE USE ASPIRATION NEEDLE 03/23/2023
OLYMPUS / GYRUS ACMI, INC. VIZISHOT 2 FLEX SINGLE USE ASPIRATION NE 01/23/2023
COOK INC COOK RETROGRADE INTUBATION SET 10/31/2022
OLYMPUS / GYRUS ACMI, INC. VIZISHOT BIOPSY NEEDLE 12/13/2021
GYRUS ACMI, INC. SINGLE USE ASPIRATION NEEDLE OLYMPUS VIZ 09/20/2021
OLYMPUS / GYRUS ACMI, INC. VIZISHOT FLEX 19 G EBUS-TBNA NEEDLE 09/08/2021
OLYMPUS / GYRUS ACMI, INC. VIZISHOT FLEX 19 G EBUS-TBNA NEEDLE 09/08/2021
GYRUS ACMI, INC SINGLE USE ASPIRATION NEEDLE 06/15/2021
-
-