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EUDAMED
FDA 510(k) incl. De Novo
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GUDID
23
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United States
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24 devices found
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Manufacturer: Implantable Devices
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Device
Device · Manufacturer · Authorizations
Verified
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Status
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Regime
Registry
Registry
Class
Class
SMITHWICK Carotid Shunt DB5000IT
Implantable Devices
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
SMITHWICK Carotid Shunt DWR1409SB
Implantable Devices
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
SMITHWICK Carotid Shunt SDS1209
Implantable Devices
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Smithwick Carotid Shunt
Implantable Devices
·
,
FDA registration: United States
FDA 510(k)
K021608
Active
Cleared 22 Oct 2002
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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