K213143 is an FDA 510(k) clearance for the Hemoclip, a Hemostatic Metal Clip For The Gi Tract (Class II — Special Controls, product code PKL), submitted by Hangzhou AGS MedTech Co., Ltd. (Hangzhou, CN). The FDA issued a Cleared decision on July 12, 2022, 288 days after receiving the submission on September 27, 2021. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.4400.
| 510(k) Number | K213143 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 27, 2021 |
| Decision Date | July 12, 2022 |
| Days to Decision | 288 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | PKL — Hemostatic Metal Clip For The Gi Tract |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 876.4400 |
| Definition | Clip Placement Within The Gastrointestinal (gi) Tract For The Purpose Of Endoscopic Marking, Hemostasis For Mucosal/sub-mucosal Defects, Bleeding Ulcers, Arteries, Polyps, Diverticula In The Colon, Prophylactic Clipping, Anchoring Feeding Tubes, Supplemental Closure Method Of Luminal Perforations. |