The following data is part of a premarket notification filed by Philips Medizinsysteme Boblingen Gmbh with the FDA for The Philips Mp20, Mp30, Mp40, Mp50, Mp60, Mp70, And Mp90 Intellivue Patient Monitors.
| Device ID | K042845 |
| 510k Number | K042845 |
| Device Name: | THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, AND MP90 INTELLIVUE PATIENT MONITORS |
| Classification | System, Network And Communication, Physiological Monitors |
| Applicant | PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Bobingen, DE D 71034 |
| Contact | Egon Pfeil |
| Correspondent | Egon Pfeil PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Bobingen, DE D 71034 |
| Product Code | MSX |
| CFR Regulation Number | 870.2300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-10-15 |
| Decision Date | 2004-11-12 |
| Summary: | summary |