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 8 of 8 Results
ProductCode: DYB Applicant: Terumo Medical Corporation Decision Date To: 01/29/2023
Results per Page
New Search  
Export all 8 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]
r2p destination slender guiding sheath Terumo Medical Corporation K193125 01/06/2020
glidesheath slender tibial pedal kit Terumo Medical Corporation K181237 08/03/2018
glidesheath slender Terumo Medical Corporation K173831 05/08/2018
destination carotid guiding sheath, destination peripheral guiding sheath, destination renal guiding sheath Terumo Medical Corporation K172995 11/21/2017
r2p destination slender guiding sheath Terumo Medical Corporation K171491 10/05/2017
glidesheath TERUMO MEDICAL CORPORATION K152173 12/01/2015
glidesheath slender Terumo Medical Corporation K142183 11/21/2014
glidesheath slender model rm* es6j10hqs, glidesheath slender model rm* es6f16hq, glidesheath slender model rm * rs6j10pq Terumo Medical Corporation K122980 12/11/2012
-
-