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

Neurovascular Liquid Embolic Agent

Unknown
FDA source (opens on fda.gov)

SGU is the FDA product code for Neurovascular Liquid Embolic Agent, a class III device type. FDA's definition for this code reads: "Arterial occlusion of the middle meningeal artery for treatment of symptomatic subdural hematoma". As of , FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code
SGU
Device name
Neurovascular Liquid Embolic Agent
FDA definition
Arterial occlusion of the middle meningeal artery for treatment of symptomatic subdural hematoma.
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
Yes
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