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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 31 Results
ProductCode: DQY Applicant: MEDTRONIC VASCULAR Decision Date To: 02/03/2023
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510(K)
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gt2 fusion guide wire, model ntlhlj180,ntlhls180, ntlhlj300, ntlhls300 MEDTRONIC VASCULAR K001969 08/16/2000
medtronic 6f taiga guiding catheter Medtronic Vascular K192296 09/20/2019
medtronioc 7f launcher biopsy guide catheter, model la7rvbb, medtronic 8f launcher biopsy catheter, model la8rvbb MEDTRONIC VASCULAR K030671 07/31/2003
model 9210 delivery catheter, model 9210 MEDTRONIC VASCULAR K013963 02/28/2002
pacific plus MEDTRONIC VASCULAR K123358 01/29/2013
selectsite c304 deflectable catheter system, models c304-s59, c304-l69, c304-xs59 & c304-xl74 MEDTRONIC VASCULAR K061416 10/25/2006
stent support guide catheter MEDTRONIC VASCULAR K010579 11/21/2001
total across MEDTRONIC VASCULAR K133539 03/26/2014
transxchange support catheter MEDTRONIC VASCULAR K033540 05/25/2004
z3 guide catheter MEDTRONIC VASCULAR K021256 05/17/2002
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