The following data is part of a premarket notification filed by Philips Medizinsysteme Boeblingen Gmbh with the FDA for Philips Intellivue Patient Monitor, Models Mp20, Mp30, Mp40, Mp50, Mp60, Mp70 And Mp90.
| Device ID | K050762 |
| 510k Number | K050762 |
| Device Name: | PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP20, MP30, MP40, MP50, MP60, MP70 AND MP90 |
| Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
| Applicant | PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 Boeblingen, Baden-wttbg, DE D-71034 |
| Contact | Egon Pfeil |
| Correspondent | Egon Pfeil PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 Boeblingen, Baden-wttbg, 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 | 2005-03-24 |
| Decision Date | 2005-04-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838072169 | K050762 | 000 |
| 00884838072152 | K050762 | 000 |
| 00884838072145 | K050762 | 000 |
| 00884838021549 | K050762 | 000 |
| 20884838072187 | K050762 | 000 |
| 20884838072170 | K050762 | 000 |