• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
51 to 60 of 500 Results *
Decision Date To: 07/22/2019
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
Results per Page
New Search  
Export all 500 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
reprocessed achieve advance mapping diagnostic electrophysiology catheter Innovative Health, LLC. K191880 12/11/2019
endotracheal tube with evacuation lumen WELL LEAD MEDICAL CO., LTD. K182739 12/11/2019
hi-torque infiltrac guide wire family Abbott Vascular K193126 12/11/2019
nemoscan Software Nemotec S.L. K192571 12/11/2019
fujifilm distal cap models 33-40 FUJIFILM Corporation K193123 12/11/2019
automated blood grouping and antibody test systems: DG Reader diagnostic grifols, s. a. BK190320 12/10/2019
health line ct cvc Health Line International Corporation K192533 12/10/2019
diode laser 808nm Beijing Superlaser Technology Co., Ltd. K192516 12/10/2019
system 1e liquid chemical sterilant processing system, system 1 endo liquid chemical sterilant processing system, model p6800, system 1 endo liquid chemical sterilant processing system, model p6900 STERIS Corporation K192929 12/10/2019
transpara Screenpoint Medical B.V. K192287 12/10/2019

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
-
-