Philips Medical Systems North America, Inc. · Class II · Cleared Sep 20, 2006
| K-number | K062283 |
| Device name | THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90 INTELLIVUE PATIENT MONITORS |
| Applicant | Philips Medical Systems North America, Inc. |
| Product code | MHX |
| Device class | Class II |
| Decision date | Sep 20, 2006 |
| Decision | Substantially Equivalent |
| Regulation | 870.1025 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov