AcuNav Volume Ultrasound Catheter
The AcuNav Volume Ultrasound Catheter provides real-time ultrasound images from inside the heart and vessels. It visualizes cardiac and great-vessel anatomy and physiology, together with…
The AcuNav Volume Ultrasound Catheter provides real-time ultrasound images from inside the heart and vessels. It visualizes cardiac and great-vessel anatomy and physiology, together with devices in the heart, during percutaneous cardiac interventions in adult and pediatric patients.
The catheter has a 12.5 French diameter, a usable length of 90 cm and four-way steering. It produces three-dimensional volume images as well as conventional two-dimensional images of the structures being examined.
Imaging Role
Its intended role is imaging guidance during the intervention. The catheter’s ultrasound views provide anatomical and device-position information; the catheter is not intended to deliver treatment.
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Philips Ultrasound (Shanghai) Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 5 |
| GE Medical Systems (China) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 57 |
| Jiangsu Tingsn Technology Co., Ltd. | Nanjing | Jiangsu | Manufacturer | 4 |
| Nanjing Shuangwei Biotechnology Co., Ltd. | Nanjing | Jiangsu | Contract manufacturer | 1 |
Record
| Listed by | Siemens Medical Solutions USA, Inc., United States |
|---|---|
| FDA product code | OBJ |
| Device type | Catheter, Ultrasound, Intravascular |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1200 |
| Establishment | Contract manufacturer, Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer |
| 510(k) | K173618 |
| Record published | 2019-02-09 |
| Record revised | 2025-02-28 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Ethylene Oxide |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | expiry date, serial number |
| Storage | Handling environment humidity 0 to 90 % RH; Storage environment temperature -10 to 50 °C |
| Sizes | Catheter gauge 12.5 Fr |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 10855958 | 12.5 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Arrow | Teleflex Medical LLC | 27 |
| Acist HDi® HD Ivus System | Acist Medical Systems, Inc. | 8 |
| Soundstar | Biosense Webster, Inc. | 6 |
| OptiCross | Boston Scientific Corporation | 4 |
| Busse Hospital Disposables | Robert Busse & Co., Inc. | 4 |
| Acist HDi® System Console | Acist Medical Systems, Inc. | 4 |
| OptiCross™ 6 | Boston Scientific Corporation | 3 |
| 7 Fr PV-Catheter | CD Leycom | 3 |
| NES Reprocessed Visions PV.014P RX Digital Ivus Catheter | North East Scientific Inc | 3 |
| OptiCross™ 6 HD | Boston Scientific Corporation | 2 |
| Acist HDi® Bed Rail Mount | Acist Medical Systems, Inc. | 2 |
| 4 Fr PV Catheter | CD Leycom | 2 |
Showing 12 of 63. All products under Catheter, Ultrasound, Intravascular
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K233270 | 2023-10-28 |
| K212959 | 2021-10-15 |
| K203726 | 2021-01-19 |
| K173618 | 2017-12-19 |
| K170263 | 2017-06-15 |
| K170992 | 2017-06-15 |
| K163478 | 2017-02-09 |
| K081808 | 2008-09-26 |
| K071234 | 2007-06-29 |
| K042593 | 2004-10-15 |
| K033650 | 2004-02-24 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Closed |
|---|---|---|---|---|---|---|
| Siemens Medical Solutions USA, Inc. | 510(k) number | 2020-05-22 | Class II | Under Investigation by firm | Due to adverse events received by the firm for left atrial perforations and Atrioventricular Node block. | 2021-10-15 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.