2 catalogue numbers from PD22130K, listed by Volcano Atheromed, Inc., United States, under Catheter, Peripheral, Atherectomy. 3 manufacturers in China are registered for this product code.
Who Else Makes It
All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for Phoenix 2.2mm x 130cm 6F Deflecting Atherectomy System | Listed by | Volcano Atheromed, Inc., United States |
| FDA product code | MCW |
| Device type | Catheter, Peripheral, Atherectomy |
| Device class | Class 2 |
| Regulation | 21 CFR 870.4875 |
| Record published | 2019-03-07 |
| Record revised | 2025-03-27 (version 6) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Keep dry; Special storage condition: Keep away from sunlight |
| Sizes | Outer diameter 2.2 mm; length 130 cm |
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.