• 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: 05/21/2019
 < 
 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]
bonine acupressure bands WellSpring Pharmaceutical Corporation K211823 09/01/2021
bonos hv genta, bonos mv genta, bonos lv genta OSARTIS GmbH K210125 03/19/2021
bonos hv, bonos mv, bonos lv Osartis GmbH K210120 03/19/2021
bravo g4 chamber autoclave SciCan Ltd. K210326 07/01/2021
callaly tampliner Calla Lily Personal Care, Ltd. K211469 06/10/2021
cannulated fasteners and nuts OsteoCentric Technologies K211290 08/03/2021
carboclear x pedicle screw system, carboclear x navigated instruments CarboFix Orthopedics Ltd. K210716 04/06/2021
cardiocurve steerable sheath Talon Surgical K210185 07/23/2021
caretaker platform, vitalstream platform, ct5 Caretaker Medical K211588 08/13/2021
catalyft pl expandable interbody system Medtronic Sofamor Danek, USA Inc. K210425 05/24/2021

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