510(k) K232955 ยท HCG Device, Neurovascular Embolization
Numen Coil Embolization System; NumenFR Detachment System
| Applicant | MicroPort NeuroTech (Shanghai) Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Jan 10, 2024 |
| Received | Sep 21, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232955
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.