510(k) K252295

Device
Ryurei
Applicant
Terumo Corporation
510(k) number
K252295
Product code
LOX
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-27
Date received
2025-07-23
Regulation
870.5100
Classification name
Catheters, Transluminal Coronary Angioplasty, Percutaneous
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Kirsten Steinmann
Address
44-1, 2-Chome, Hatagaya Shibuya-Ku Tokyo JP 151-0072 151-0072

FDA Registration Numbers

Source Documents

510(k) summary PDF

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