Clear-Jet Injection Catheter
FDA 510(k) K181690 · Finemedix Co., Ltd.
510(k) numberK181690
Submission
- Device name
- Clear-Jet Injection Catheter
- Applicant
- Finemedix Co., Ltd.
Daegu, KR - Received
- June 26, 2018
- Decision date
- December 21, 2018
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FBK – Endoscopic Injection Needle, Gastroenterology-Urology
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Specialty
- Gastroenterology, Urology
inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.
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|---|---|---|---|
| K260262 | Injection NeedleFBK · Traditional | Mirco-Tech (Nanjing) Co., Ltd. | 05/29/2026SE |
| K253598 | InjecSURE Injection SystemFBK · Traditional | Carbon Medical Technologies, Inc. | 03/31/2026SE |
| K252021 | Disposable Endoscopic Injection NeedlesFBK · Traditional | Changzhou New Med Micro-Medtech Co., Ltd. | 12/02/2025SE |
| K252247 | Injector Force Max Single Use Injector (NM-400L); Injector Force Max Single Use Injector…FBK · Traditional | Olympus Medical Systems Corporation | 10/16/2025SE |
| K241595 | EzVu Visual Vasopressor injector (EV-19)FBK · Traditional | Veol Medical Technologies Pvt , Ltd. | 02/27/2025SE |
| K240675 | Endoscopic Injection NeedlesFBK · Traditional | Promisemed Hangzhou Meditech Co., Ltd. | 10/04/2024SE |
| K241523 | injeTAK Adjustable Tip Needle (DIS199; DIS201)FBK · Special | Laborie Medical Technologies, Corp. | 08/27/2024SE |
| K232200 | Disposable Injection NeedlesFBK · Traditional | Ningbo Xinwell Medical Technology Co., Ltd. | 04/12/2024SE |
| K232826 | Articulator Injection Needle (00711807), Articulator Injection Needle (00711810)…FBK · Traditional | Steris | 03/08/2024SE |
| K232442 | Disposable Endoscope Injection NeedlesFBK · Traditional | Zhejiang Soudon Medical Technology Co., Ltd. | 11/09/2023SE |
More from Zhejiang Soudon Medical Technology Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K251478 | ClearTip TBNA TypeKTI · Traditional | 04/16/2026SE |
| K250994 | ClearTip FNA and FNB TypesFCG · Traditional | 08/21/2025SE |
| K242857 | ClearHemograsperKGE · Traditional | 05/21/2025SE |
| K242134 | ClearCap Distal AttachmentOCX · Special | 08/20/2024SE |
| K231267 | ClearTipFCG · Traditional | 06/30/2023SE |
| K202616 | ClearCap Distal AttachmentOCX · Traditional | 02/19/2021SE |
| K200217 | ClearEndoclipPKL · Traditional | 10/05/2020SE |
| K183021 | ClearEndoclipPKL · Traditional | 06/28/2019SE |
| K183289 | ClearGrasp SnareFDI · Traditional | 03/06/2019SE |
| K180363 | Clear-Tip EUS-FNAFCG · Traditional | 11/01/2018SE |
Questions and answers
When was Clear-Jet Injection Catheter cleared by the FDA?
Clear-Jet Injection Catheter (K181690) received a 510(k) decision of Substantially Equivalent on December 21, 2018, 178 days after the submission was received.
What is the product code of K181690?
The FDA product code is FBK – Endoscopic Injection Needle, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.