510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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SEQClass III

Covered Stent Vascular Connector, Hemodialysis Access Circuit

Unknown
FDA source (opens on fda.gov)

SEQ is the FDA product code for Covered Stent Vascular Connector, Hemodialysis Access Circuit, a class III device type. FDA's definition for this code reads: "The device is intended for suture-less attachment between an arteriovenous (AV) graft to a native vessel or between two native vessels (i.e., lack of suture placement on one or both ends) for the creation of a hemodialysis access site". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
SEQ
Device name
Covered Stent Vascular Connector, Hemodialysis Access Circuit
FDA definition
The device is intended for suture-less attachment between an arteriovenous (AV) graft to a native vessel or between two native vessels (i.e., lack of suture placement on one or both ends) for the creation of a hemodialysis access site.
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
0

Companies listing this code with FDA

Companies whose registered establishments list this code