Philips Medizin Systeme Boeblingen GmbH · Class II · Cleared Nov 26, 2013
| K-number | K131913 |
| Device name | INTELLIVUE CL SPO2 POD AND CL NBP POD, PHILIPS INTELLIVUE PATIENT MONITORS MP5, MP5T, MP5SC |
| Applicant | Philips Medizin Systeme Boeblingen GmbH |
| Product code | DRG |
| Device class | Class II |
| Decision date | Nov 26, 2013 |
| Decision | Substantially Equivalent |
| Regulation | 870.2910 |
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