• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 > 
 
74 records meeting your search criteria returned- Product Code: FNM Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARJOHUNTLEIGH, INC. MAXXAIR ETS 03/20/2023
ARJO (SUZHOU) CO., LTD. AURALIS 03/17/2023
ARJOHUNTLEIGH POLSKA SP. Z O.O. NIMBUS PROFESSIONAL 01/19/2023
ARJOHUNTLEIGH, INC. MAXXAIR ETS 01/16/2023
ARJOHUNTLEIGH, INC. FIRST STEP SELECT PUMP 12/12/2022
JOERNS HEALTHCARE DERMAFLOAT LAL 12/09/2022
ARJO (SUZHOU) CO., LTD. AUTO LOGIC 12/06/2022
ARJO (SUZHOU) CO., LTD. AUTO LOGIC 11/04/2022
ARJO (SUZHOU) CO., LTD. NIMBUS 4 11/02/2022
ARJO (SUZHOU) CO., LTD. AUTO LOGIC 10/25/2022
-
-