Catalogue number 10444868, listed by Siemens Healthcare Diagnostics Products GmbH, Germany, under System, Automated Platelet Aggregation. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Zhejiang. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for PFA-100® System | Listed by | Siemens Healthcare Diagnostics Products GmbH, Germany |
| FDA product code | JOZ |
| Device type | System, Automated Platelet Aggregation |
| Device class | Class 2 |
| Regulation | 21 CFR 864.5700 |
| Establishment | Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer |
| 510(k) | K060489 |
| Record published | 2016-09-24 |
| Record revised | 2022-09-16 (version 5) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Label carries | serial number |
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.