Angio-Flo Continuous Arterial Cath Flush Device
FDA 510(k) K860570 · Parke-Davis Co.
510(k) numberK860570
Submission
- Device name
- Angio-Flo Continuous Arterial Cath Flush Device
- Applicant
- Parke-Davis Co.
Rochester, MI, US - Received
- February 14, 1986
- Decision date
- March 31, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- KRA – Catheter, Continuous Flush
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1210
- Specialty
- Cardiovascular
Other 510(k)s with product code KRA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254051 | Extroducer Infusion Catheter SystemKRA · Traditional | SmartWise Sweden AB | 09/11/2026SE |
| K261610 | Verge MicrocatheterKRA · Special | Instylla, Inc. | 06/11/2026SE |
| K260771 | TruSelect 2.6 MicrocatheterKRA · Special | Boston Scientific Corporation | 05/15/2026SE |
| K250794 | InVera Infusion DeviceKRA · Traditional | Invera Medical | 03/12/2026SE |
| K243534 | Micro CatheterKRA · Traditional | Suzhou Zenith Vascular SciTech Limited | 07/30/2025SE |
| K231821 | XO Cath Microcatheter (E20-090-S, E20-110-S, E20-130-S, E20-150-S, E20-175-S, E20-220-S…KRA · Traditional | Transit Scientific, LLC | 11/29/2023SE |
| K231279 | Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mmKRA · Traditional | Ablative Solutions, Inc. | 07/05/2023SE |
| K231148 | ScleroSafe 150 mm, ScleroSafe 350 mmKRA · Traditional | Vvt Medical , Ltd. | 06/20/2023SE |
| K230957 | TriSalus TriNav® LV Infusion SystemKRA · Traditional | Trisalus Life Sciences | 05/02/2023SE |
| K223139 | Wallaby 017 Micro CatheterKRA · Traditional | Wallaby Medical | 04/25/2023SE |
More from Wallaby Medical
| 510(k) | Device | Decision |
|---|---|---|
| K861725 | Intracath Intravenous Catheter Placement UnitFOZ · Traditional | 12/04/1986SE |
| K862119 | Deseret Flo-Thru Injectate Temperature SensorDYG · Traditional | 08/29/1986SE |
| K855120 | Ati Disposable Biological Test PackFRC · Traditional | 06/18/1986SE |
| K860290 | Viapic Central Line CatheterFOZ · Traditional | 03/18/1986SE |
| K852192 | Disposable Steam Biological Test PackFRC · Traditional | 11/01/1985SE |
| K841967 | Deseret Thermodilution Cardiac OutputDXG · Traditional | 08/19/1985SE |
| K851327 | Deseret Arterial CatheterFOZ · Traditional | 06/14/1985SE |
| K852078 | Spectrum(Tentative)FOZ · Traditional | 06/07/1985SE |
| K844840 | Deseret Introducer SetDYB · Traditional | 05/16/1985SE |
| K850505 | Deseret Epidural Catheter W/Toughy-Borst AdapterBSO · Traditional | 03/11/1985SE |
Questions and answers
When was Angio-Flo Continuous Arterial Cath Flush Device cleared by the FDA?
Angio-Flo Continuous Arterial Cath Flush Device (K860570) received a 510(k) decision of Substantially Equivalent on March 31, 1986, 45 days after the submission was received.
What is the product code of K860570?
The FDA product code is KRA – Catheter, Continuous Flush, a Class II (moderate risk) device regulated under 21 CFR 870.1210.