Acute Dual Lumen Hemodialysis Catheter— 510(k) K200426
UnknownHealth Line International Corporation
FDA 510(k) clearance K200426 for Acute Dual Lumen Hemodialysis Catheter, Unknown on 2020-12-24. Applicant: Health Line International Corporation. Device class: 2.
Clearance details
- Applicant
- Health Line International Corporation
- Product code
- Code MPB
- Device class
- Class 2
- Regulation
- 21 CFR 876.5540
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Recent devices under product code MPB
view all- K250836 — 14F Duo-Flow® Side X Side Double Lumen Catheter
- K192807 — Duo-Flow Side x Side Double Lumen Catheter
- K192302 — Mahurkar Acute Single Lumen Catheter, Mahurkar Acute Dual Lumen Catheter, Mahurkar Acute Triple Lumen Catheter, Mahurkar Acute High Pressure Triple Lumen Catheter
- K163458 — Zenysis Short-Term Dialysis Catheter
- K161504 — Cook Turbo-Flo HD Acute Hemodialysis Catheter Set/Tray
More clearances from Health Line International Corporation
view allAdverse events under product code MPB
product code MPB- Death
- 18
- Malfunction
- 1,042
- Total
- 1,060
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.