510(k) K222170 ยท NIE Catheter, Hemodialysis, Triple Lumen, Non-Implanted
Power Acute Triple Lumen Hemodialysis Catheter
| Applicant | Health Line International Corporation, Slat Lake City UT, US |
| Decision | Substantially Equivalent, Jan 13, 2023 |
| Received | Jul 21, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222170
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.