INTELLIVUE PATIENT MONITOR, MODELS MP2, X2, MP5, MP5T, MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90, & MX800— 510(k) K102562

Substantially Equivalent

Philips Medizin Systeme Boblingen GmbH

FDA 510(k) clearance K102562 for INTELLIVUE PATIENT MONITOR, MODELS MP2, X2, MP5, MP5T, MP20, MP30, MP40, MP50, MP60, MP70, MP80, MP90, & MX800, Substantially Equivalent on 2010-10-21. Applicant: Philips Medizin Systeme Boblingen GmbH.

Clearance details

Applicant: Philips Medizin Systeme Boblingen GmbH
Product code: Code MHX
Advisory panel: Cardiovascular
Date received: 2010-09-07
Decision date: 2010-10-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Boblingen, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code MHX

product code MHX

Death: 580
Injury: 2,441
Malfunction: 12,655
Other: 3
Total: 15,679

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.