FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Ryurei

K Number: K252295 · Decision Mar 27, 2026
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
85
Applicant Total
13
Review Days
247

Basic Information

Device Name
Ryurei
K Number
K252295
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5100
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Terumo Corporation
Date Received
July 23, 2025
Decision Date
March 27, 2026
Product Code
LOX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous

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