Philips Medical System Nederland B.V.
Philips Medical System Nederland B.V. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record.
- Latest 510(k)
- Dec 17, 2020
Reviewing Philips Medical System Nederland B.V. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Or get Philips Medical System Nederland B.V.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 1 | Oct 4, 2026 | Not stated | Current |
| Inspections | 0 | Oct 23, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K201081 | AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter | Dec 17, 2020 |