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

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
121 to 130 of 500 Results *
Decision Date To: 11/29/2022
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
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]
cervical plate system Double Medical Technology Inc. K223753 03/14/2023
rt elements (4.0) Brainlab AG K223279 03/14/2023
leg and foot air wave pressure therapy device Zhangzhou Easepal Innovation Co Ltd. K223464 03/14/2023
jett plasma medical ii Compex, Spol. s.r.o K213247 03/14/2023
sofwave system Sofwave Medical Ltd. K230019 03/14/2023
surgical face mask Wuhan Huashida Protective Products Co., Ltd. K221352 03/13/2023
remi robotic navigation system Fusion Robotics, LLC K223350 03/13/2023
innova vision hydrogel (etafilcon a) soft (hydrophilic) contact lens Innova Vision Inc. K222954 03/13/2023
aarhus applicator set Varian Medical Systems, Inc K222775 03/13/2023
omnia medical coupler-c anterior cervical plate Omnia Medical, LLC K223321 03/13/2023

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