Duo-Flow Side x Side Double Lumen Catheter
FDA 510(k) K192807 · Medical Components, Inc. (dba MedComp)
510(k) numberK192807
Submission
- Device name
- Duo-Flow Side x Side Double Lumen Catheter
- Applicant
- Medical Components, Inc. (dba MedComp)
Harleysville, PA, US - Received
- October 1, 2019
- Decision date
- April 23, 2020
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MPB – Catheter, Hemodialysis, Non-Implanted
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5540
- Specialty
- Gastroenterology, Urology
- Life-sustaining
- Yes
Other 510(k)s with product code MPB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K250836 | 14F Duo-Flow® Side X Side Double Lumen CatheterMPB · Traditional | Medical Components, Inc. | 08/12/2025SE |
| K200426 | Acute Dual Lumen Hemodialysis CatheterMPB · Traditional | Health Line International Corporation | 12/24/2020SESK |
| K192302 | Mahurkar Acute Single Lumen Catheter, Mahurkar Acute Dual Lumen Catheter, Mahurkar Acute…MPB · Traditional | Covidien, LLC | 01/17/2020SEKD |
| K163458 | Zenysis Short-Term Dialysis CatheterMPB · Traditional | C.R. Bard, Inc. | 04/04/2017SEKD |
| K161504 | Cook Turbo-Flo HD Acute Hemodialysis Catheter Set/TrayMPB · Special | Cook Incorporated | 01/06/2017SEKD |
| K153190 | Zenysis Short-Term Dialysis CatheterMPB · Traditional | C.R. Bard, Inc. | 01/05/2016SE |
| K122091 | Cook Turbo-Flo HD Acute Hemodialysis Catheter Set/Tray Cook Spectrum Turbo-Flo HD Acute…MPB · Traditional | Cook, Inc. | 07/29/2013SESK |
| K120674 | Mahurkar Elite Acute Dual Lumen Catheter, Elite Acute Triple Lumen CatheterMPB · Special | Covidien | 04/04/2012SESK |
| K110793 | Amecath and Amecath Uniqath Soft Short Term Dual Hemodialysis Catheterization KitsMPB · Traditional | Ameco Medical Industries | 12/16/2011SE |
| K102833 | Disposable Hemodialysis Access Catheter SetsMPB · Traditional | Foshan Nanhai Bai HE Medical Technology Co., Ltd. | 11/18/2011SE |
More from Foshan Nanhai Bai HE Medical Technology Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K232945 | Trio-CT® Triple Lumen Catheter w/ Curved ExtensionsNIE · Traditional | 11/16/2023SESK |
| K202176 | Symetrex LTHD Catheter, Symetrex LTHD Catheter with SideholesMSD · Special | 09/03/2020SE |
| K183219 | Trio-CT Triple Lumen CatheterNIE · Traditional | 06/14/2019SEKD |
| K181175 | 12F Tri-Flow Triple Lumen CatheterNIE · Traditional | 07/05/2018SESK |
| K173667 | 15.5F X 19 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 23 cm…MSD · Traditional | 05/17/2018SESK |
| K180567 | C3 Wave SystemLJS · Special | 04/12/2018SE |
| K170934 | C3 Wave SystemLJS · Traditional | 12/06/2017SE |
| K170770 | CT MidlinePND · Special | 07/25/2017SE |
Questions and answers
When was Duo-Flow Side x Side Double Lumen Catheter cleared by the FDA?
Duo-Flow Side x Side Double Lumen Catheter (K192807) received a 510(k) decision of Substantially Equivalent on April 23, 2020, 205 days after the submission was received.
What is the product code of K192807?
The FDA product code is MPB – Catheter, Hemodialysis, Non-Implanted, a Class II (moderate risk) device regulated under 21 CFR 876.5540.