510(k) K260508

Device
LOBO Vascular Occlusion System
Applicant
Okami Medical, Inc.
510(k) number
K260508
Product code
KRD
Decision
Substantially Equivalent (SESE)
Decision date
2026-04-10
Date received
2026-02-17
Regulation
870.3300
Classification name
Device, Vascular, For Promoting Embolization
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Cora Sim
Address
8 Argonaut Suite 100 Aliso Viejo CA US 92656 92656

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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K242608Embozene Color-Advanced MicrospheresVarian Medical Systems, Inc.2025-01-17
K240873TEMBO Embolic SystemInstylla, Inc.2024-12-16
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K242507OBSIDIO™ Conformable EmbolicBoston Scientific2024-10-03
K232934SunsphereHangzhou Yangshun Medical Technology Co.,Ltd2024-05-30
K240261Siege Vascular Plug (SVP2.5-0.021); Siege Vascular Plug (SVP4-0.021); Siege Vascular Plug (SVP6-0.027)Merit Medical Systems, Inc.2024-05-02