• 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
-
131 to 140 of 500 Results *
Decision Date To: 11/29/2022
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
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]
high protection surgical gown 3A Medical Products Co., Ltd K222456 03/12/2023
arthrex knotless fibertak suture anchor Arthrex Inc. K230433 03/10/2023
avoset infusion pump system Eitan Medical Ltd. K213744 03/10/2023
aristotle 14 guidewire; aristotle 18 guidewire; aristotle 24 guidewire; volo 14 guidewire; zoom wire 14 guidewire Scientia Vascular, LLC K220398 03/10/2023
vial adapter Hangzhou Qiantang Longyue Biotechnology Co., LTD K222718 03/10/2023
attune® revision cones DePuy Ireland UC K230295 03/10/2023
bd vacutainer® luer-lok™ access device, bd vacutainer® blood transfer device Becton Dickinson and Company K222478 03/10/2023
lntravascular administration sets with stopcock and manifold Baxter Healthcare Corporation K223175 03/10/2023
umi panorama Shanghai United Imaging Healthcare Co., Ltd. K223325 03/10/2023
uni knee resurfacing system Overture Resurfacing Inc. K221292 03/10/2023

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