THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, AND MP90 INTELLIVUE PATIENT MONITORS— 510(k) K042845
Substantially EquivalentPhilips Medizin Systeme Boblingen GmbH
FDA 510(k) clearance K042845 for THE PHILIPS MP20, MP30, MP40, MP50, MP60, MP70, AND MP90 INTELLIVUE PATIENT MONITORS, Substantially Equivalent on 2004-11-12. Applicant: Philips Medizin Systeme Boblingen GmbH.
Clearance details
- Applicant
- Philips Medizin Systeme Boblingen GmbH
- Product code
- Code MSX
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Boblingen, DE
Adverse events under product code MSX
product code MSX- Death
- 59
- Total
- 59
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.