The following data is part of a premarket notification filed by Philips Medizinsysteme Boeblingen Gmbh with the FDA for The Philips Mp20, Mp30, Mp40, Mp50, Mp60, Mp70 And Mp90 Intellivue Patient Monitors.
| Device ID | K050141 |
| 510k Number | K050141 |
| Device Name: | THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70 AND MP90 INTELLIVUE PATIENT MONITORS |
| Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
| Applicant | PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 Boeblingen, DE D 71034 |
| Contact | Hauke Schik |
| Correspondent | Hauke Schik PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 Boeblingen, DE D 71034 |
| Product Code | MHX |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-01-25 |
| Decision Date | 2005-02-11 |
| Summary: | summary |