Philips Image Guided Therapy Corporation
Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of PhilipsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
- 510(k) clearances: 4
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
Latest Records
Newest first across sources; each opens the record| Date | Record | Source |
|---|---|---|
| Feb 24, 2026 | IntraSight PlusK253714 · IYO | 510(k) clearances |
| May 9, 2025 | VeriSight Intracardiac Echocardiography Catheter (VSICE2D); VeriSight Pro Intracardiac Echocardiography Catheter (VSICE3D)K251103 · OBJ | 510(k) clearances |
| Sep 2, 2020 | VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE CatheterK200812 · OBJ | 510(k) clearances |
| May 22, 2020 | Reconnaissance PV .018 OTW Digital IVUS CatheterK200410 · OBJ | 510(k) clearances |
Canada and Imports
Matched by company name- Active Health Canada device licences
- 18, as of Nov 10, 2026
Names and Identifiers
- Appears as
- Website
- philips.com
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built