K222170 is an FDA 510(k) clearance for the Power Acute Triple Lumen Hemodialysis Catheter. This device is classified as a Catheter, Hemodialysis, Triple Lumen, Non-implanted (Class II - Special Controls, product code NIE).
Submitted by Health Line International Corporation (Slat Lake City, US). The FDA issued a Cleared decision on January 13, 2023, 176 days after receiving the submission on July 21, 2022.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5540. Short-term (< 30 Days) Central Venous Access For Hemodialysis And Apheresis, With A Third Lumen For Infusion..
| 510(k) Number | K222170 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 21, 2022 |
| Decision Date | January 13, 2023 |
| Days to Decision | 176 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | NIE - Catheter, Hemodialysis, Triple Lumen, Non-implanted |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.5540 |
| Definition | Short-term (< 30 Days) Central Venous Access For Hemodialysis And Apheresis, With A Third Lumen For Infusion. |