510(k) K192399 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Infinity Angioplasty Balloon Catheter
| Applicant | Infinity Angioplasty Balloon Company, LLC, Toledo OH, US |
| Decision | Substantially Equivalent, May 20, 2020 |
| Received | Sep 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192399
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.