FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

TIANYI Extracorporeal Blood Tubing Set (TY-NDEO-A1)

K Number: K251442 · Decision Oct 2, 2025
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
76
Applicant Total
3
Review Days
146

Basic Information

Device Name
TIANYI Extracorporeal Blood Tubing Set (TY-NDEO-A1)
K Number
K251442
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ningbo Tianyi Medical Appliance Co., Ltd.
Date Received
May 9, 2025
Decision Date
October 2, 2025
Product Code
FJK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FJK Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

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