Philips Medical Systems Nederland B.V. · Class II · Cleared Oct 2, 2025
| K-number | K251215 |
| Device name | Philips IntelliSpace Cardiovascular |
| Applicant | Philips Medical Systems Nederland B.V. |
| Product code | LLZ |
| Device class | Class II |
| Decision date | Oct 2, 2025 |
| Decision | Substantially Equivalent |
| Regulation | 892.2050 |
The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →
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