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

Injection Needle

K Number: K260262 · Decision May 29, 2026
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
88
Applicant Total
5
Review Days
121

Basic Information

Device Name
Injection Needle
K Number
K260262
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mirco-Tech (Nanjing) Co., Ltd.
Date Received
January 28, 2026
Decision Date
May 29, 2026
Product Code
FBK
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
FBK Endoscopic Injection Needle, Gastroenterology-Urology

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