Pulsar Vascular Inc

FDA Filings

This page includes the latest FDA filings for Pulsar Vascular Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3008680601
FEI Number3008680601
NamePULSAR VASCULAR INC.
Owner & OperatorPulsar Vascular Inc.
Contact Address130 Knowles Drive Suite E
Los Gatos CA 95032 US
Official Correspondent
  • Hannah Foley
  • x-786-4942755-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address130 Knowles Dr Ste E
Los Gatos, CA 95032 US
Establishment Type
  • Manufacture Device in the United States for Export Only
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
PULSAR VASCULAR, INC.
PulseRider Aneurysm Neck Reconstruction Device Connection Cable PRDSACD2019-09-25
PULSAR VASCULAR, INC.
PulseRider Aneurysm Neck Reconstruction Device Detachment System PRDSCBD2019-09-25
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 201-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 203-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 211-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 301-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 303-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 311-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 313-D2019-09-18
PULSAR VASCULAR, INC.
Pulsar Vascular PulseRider Aneurysm Neck Reconstruction Device 213-D2018-07-06
PULSAR VASCULAR INC.
PulseRider Aneurysm Neck Reconstruction Device2017-06-22
PULSAR VASCULAR INC.
PulseRider Aneurysm Neck Reconstruction Device2012-03-07

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