← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS III

SGU — Neurovascular Liquid Embolic Agent

Arterial occlusion of the middle meningeal artery for treatment of symptomatic subdural hematoma.

DEVICE CLASS
Class III
MEDICAL SPECIALTY
Unknown
REVIEW PANEL
NE
✓ Implant✓ Life-sustaining— GMP-exempt— Third-party review eligible
3
510(K)/PMA CLEARANCES
pma: 3
0
RECALL ENTRIES

Recent clearances

P250009Balt USA, LLC · pma2026-01-30
P990040Cerenovus, Inc. · pma2025-12-16
P030004Ev3 Neurovascular · pma2025-12-08

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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