FDA Device Establishments · JSON-LD · Markdown
FEI 3008363989 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3008363989 |
|---|---|
| Owner / Operator | Philips Medical Systems International BV (#2939520) |
| Address | 3721 Valley Centre Dr Ste 500, San Diego, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 3 |
| Product codes (top 20) | DQO, DQX, DQK |
| Regulation § (21 CFR) | 870.1200, 870.1330, 870.1425 |
| Proprietary names | AltaTrack Guidewire; AltaTrack equipment R1 |
Source: openFDA. Public-domain (CC0).