FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Disposable Hot Biopsy Forceps
K Number: K231721
·
Decision Dec 14, 2023
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
45
Applicant Total
6
Review Days
184
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Basic Information
- Device Name
- Disposable Hot Biopsy Forceps
- K Number
- K231721
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.4300
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Beijing Zksk Technology Co., Ltd.
- Date Received
- June 13, 2023
- Decision Date
- December 14, 2023
- Product Code
- KGE
- 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 |
|---|---|---|---|
| KGE | Forceps, Biopsy, Electric | FDA class 2 | Gastroenterology, Urology |
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Other Clearances by Beijing Zksk Technology Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K242192 | Disposable Sphincterotome | Feb 6, 2025 | Substantially Equivalent |
| K213217 | Disposable hemoclip | Nov 14, 2022 | Substantially Equivalent |
| K213222 | Disposable Polypectomy Snare | Jun 6, 2022 | Substantially Equivalent |
| K213223 | Multi-Band Ligator | Jun 6, 2022 | Substantially Equivalent |
| K213239 | Endoscopic Injection Needle | Jun 2, 2022 | Substantially Equivalent |