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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 19 of 19 Results
ProductCode: DYB Applicant: TERUMO MEDICAL CORP. Decision Date To: 04/24/2024
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Export all 19 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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carotid access kit TERUMO MEDICAL CORP. K060666 06/29/2006
destination carotid guiding sheath TERUMO MEDICAL CORP. K052185 09/06/2005
pinnacle destination peripheral guiding sheath TERUMO MEDICAL CORP. K051601 08/04/2005
renal guiding sheath TERUMO MEDICAL CORP. K012854 11/21/2001
carotid guiding sheath TERUMO MEDICAL CORP. K012812 11/14/2001
pinnacle r/o ii or radifocus introducer ii TERUMO MEDICAL CORP. K003424 11/21/2000
pinnacle r/o or redifocus introducer r/o (comprised of a sheath & dilator) TERUMO MEDICAL CORP. K984260 01/26/1999
radifocus introducer ii kit TERUMO MEDICAL CORP. K954234 11/27/1995
terumo radifocus introducer kit TERUMO MEDICAL CORP. K863139 10/10/1986
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