FDA Device Establishments · JSON-LD · Markdown
FEI 3007635982 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3007635982 |
|---|---|
| Owner / Operator | Confluent Medical Technologies, Inc. (#10033958) |
| Address | 47533 Westinghouse Dr, Fremont, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DQX |
| Regulation § (21 CFR) | 870.1330 |
| Proprietary names | Aquatrack Hydrophilic Nitinol Guidewire |
Source: openFDA. Public-domain (CC0).