FDA Device Establishments · JSON-LD · Markdown
FEI 3042970803 · Manufacture Medical Device · Status: Active
| FEI Number | 3042970803 |
|---|---|
| Owner / Operator | Leadoptik Inc. (#10094418) |
| Address | 2380 Qume Dr Ste A, San Jose, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KTI |
| Regulation § (21 CFR) | 874.4680 |
| Proprietary names | LIA-1 Catheter |
Source: openFDA. Public-domain (CC0).