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
-
1 to 10 of 19 Results
ProductCode: DQY Applicant: CONCENTRIC MEDICAL, INC. Decision Date To: 05/04/2024
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 19 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]
modified hd guide catheter CONCENTRIC MEDICAL, INC. K133177 02/25/2014
modified concentric microcatheter CONCENTRIC MEDICAL, INC. K131437 10/11/2013
modified flowgate balloon guide catheter CONCENTRIC MEDICAL, INC. K131492 10/03/2013
modified balloon guide catheter model 90253, 90254 CONCENTRIC MEDICAL, INC. K122581 11/21/2012
concentric balloon guide catheter CONCENTRIC MEDICAL, INC. K112404 03/15/2012
modified hd guide catheter CONCENTRIC MEDICAL, INC. K110483 04/04/2011
concentric balloon guide catheter CONCENTRIC MEDICAL, INC. K102657 11/17/2010
modification to modified hd guide catheter CONCENTRIC MEDICAL, INC. K092298 11/05/2009
hd guide catheter CONCENTRIC MEDICAL, INC. K090335 05/06/2009
modified hd guide catheter CONCENTRIC MEDICAL, INC. K080583 07/18/2008
-
-