ClearHemograsper
FDA 510(k) K242857 · Finemedix Co., Ltd.
510(k) numberK242857
Submission
- Device name
- ClearHemograsper
- Applicant
- Finemedix Co., Ltd.
Daegu, KR - Received
- September 20, 2024
- Decision date
- May 21, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KGE – Forceps, Biopsy, Electric
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.4300
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code KGE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251807 | Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LRKGE · Traditional | Olympus Medical Systems Corp. | 03/06/2026SE |
| K250187 | Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)KGE · Traditional | Olympus Medical Systems Corporation | 10/07/2025SE |
| K231721 | Disposable Hot Biopsy ForcepsKGE · Traditional | Beijing Zksk Technology Co., Ltd. | 12/14/2023SE |
| K220053 | Diathermic Slitter (FlushKnife) DK2620JI and DK2623JIKGE · Special | Fujifilm Corporation | 02/04/2022SE |
| K210406 | Bipolar Coagulation ForecepsKGE · Traditional | Hangzhou AGS MedTech Co., Ltd. | 10/05/2021SE |
| K202438 | Ensure Single-Use Coagulation ForcepsKGE · Traditional | Micro-Tech (Nanjing) Co., Ltd. | 03/15/2021SE |
| K183428 | Avulsion ForcepsKGE · Traditional | STERIS Corporation | 04/16/2019SE |
| K180018 | Disposable Hot Biopsy ForcepsKGE · Traditional | Micro-Tech (Nanjing) Co., Ltd. | 07/05/2018SE |
| K180134 | Ensizor Monopolar Endoscopic ScissorsKGE · Traditional | Slater Endoscopy, LLC | 06/29/2018SE |
| K171973 | Captura® Disposable Hot Biopsy ForcepsKGE · Traditional | Wilson-Cook Medical, Inc. | 03/21/2018SE |
More from Wilson-Cook Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K251478 | ClearTip TBNA TypeKTI · Traditional | 04/16/2026SE |
| K250994 | ClearTip FNA and FNB TypesFCG · Traditional | 08/21/2025SE |
| 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 |
| K181690 | Clear-Jet Injection CatheterFBK · Traditional | 12/21/2018SE |
| K180363 | Clear-Tip EUS-FNAFCG · Traditional | 11/01/2018SE |
Questions and answers
When was ClearHemograsper cleared by the FDA?
ClearHemograsper (K242857) received a 510(k) decision of Substantially Equivalent on May 21, 2025, 243 days after the submission was received.
What is the product code of K242857?
The FDA product code is KGE – Forceps, Biopsy, Electric, a Class II (moderate risk) device regulated under 21 CFR 876.4300.