K232970 is an FDA 510(k) clearance for the Hem-o-lok® Ligating Clips. This device is classified as a Clip, Implantable (Class II - Special Controls, product code FZP).
Submitted by Teleflex Medical (Morrisville, US). The FDA issued a Cleared decision on January 12, 2024, 113 days after receiving the submission on September 21, 2023.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4300.
| 510(k) Number | K232970 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 21, 2023 |
| Decision Date | January 12, 2024 |
| Days to Decision | 113 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FZP — Clip, Implantable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4300 |