510(k) K203390 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
Artimes pro Balloon Dilatation Catheter
| Applicant | Brosmed Medical Co., Ltd., Dongguan, CN |
| Decision | Substantially Equivalent, Apr 14, 2021 |
| Received | Nov 18, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203390
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.