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 | Device Class | Medical Specialty |
|---|---|---|---|
| FBK | Endoscopic Injection Needle, Gastroenterology-Urology | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Mirco-Tech (Nanjing) Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K253832 | Dilation Balloon Catheter | Apr 24, 2026 | Substantially Equivalent |
| K254153 | Single-use Video Scope; PB Digital Controller | Apr 3, 2026 | Substantially Equivalent |
| K253139 | Disposable Distal Cap | Mar 19, 2026 | Substantially Equivalent |
| K233772 | Disposable Dual Action Tissue Closure Device | Mar 19, 2024 | Substantially Equivalent |