510(k) K202231 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
JADE
| Applicant | OrbusNeich Medical (Shenzhen) Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Dec 10, 2020 |
| Received | Aug 7, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202231
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.