510(k) K230374 · LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
Coronary Dilatation Balloon Catheter (VesPenetrator®), Coronary Dilatation Balloon Catheter (VesTraveler®), Coronary Dilatation Balloon Catheter (VexPander®)
| Applicant | Dongguan TT Medical, Inc., Dongguan, CN |
| Decision | Substantially Equivalent, Jun 29, 2023 |
| Received | Feb 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230374
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.