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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 19 Results
ProductCode: DYB Applicant: TERUMO MEDICAL CORP. Decision Date To: 04/24/2024
 
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510(K)
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pinnacle precision access system TERUMO MEDICAL CORP. K111606 10/03/2011
glidesheath TERUMO MEDICAL CORP. K102008 07/21/2010
pinnacle destination peripheral guiding sheath TERUMO MEDICAL CORP. K091329 05/29/2009
pinnacle roii introducer sheath TERUMO MEDICAL CORP. K082847 10/29/2008
glidesheath TERUMO MEDICAL CORP. K082644 09/18/2008
destination renal guiding sheath TERUMO MEDICAL CORP. K081045 05/28/2008
pinnacle destination peripheral guiding sheath TERUMO MEDICAL CORP. K081046 05/21/2008
device modification to pinnacle destination peripheral guiding sheath TERUMO MEDICAL CORP. K080415 03/07/2008
modification to pinnacle roii hiflow introducer sheath TERUMO MEDICAL CORP. K062446 10/23/2006
modification to glidesheath TERUMO MEDICAL CORP. K062858 10/20/2006
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