FDA Device Establishments · JSON-LD · Markdown
FEI 1035166 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 1035166 |
|---|---|
| Owner / Operator | OSCOR INC. (#1035166) |
| Address | 4875 Palm Harbor Blvd, PALM HARBOR, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LDF |
| Regulation § (21 CFR) | 870.3680 |
| Proprietary names | TEMPORARY PACING PRODUCTS |
Source: openFDA. Public-domain (CC0).