510(k) K253361 ยท DQY Catheter, Percutaneous
Teleport Glide Microcatheter
| Applicant | OrbusNeich Medical (Shenzhen) Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Apr 10, 2026 |
| Received | Sep 30, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253361
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.