510(k) K200426 ยท MPB Catheter, Hemodialysis, Non-Implanted
Acute Dual Lumen Hemodialysis Catheter
| Applicant | Health Line International Corporation, Salt Lake City UT, US |
| Decision | Unknown, Dec 24, 2020 |
| Received | Feb 21, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200426
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.