THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20— 510(k) K031481

Substantially Equivalent

Philips Medizin Systeme Boblingen GmbH

FDA 510(k) clearance K031481 for THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20, Substantially Equivalent on 2003-05-29. Applicant: Philips Medizin Systeme Boblingen GmbH.

Clearance details

Applicant: Philips Medizin Systeme Boblingen GmbH
Product code: Code MHX
Advisory panel: Cardiovascular
Date received: 2003-05-12
Decision date: 2003-05-29
Decision: Substantially Equivalent
Clearance type: Special
Location: Boeblingen, Baden-Wuerttemberg, DE

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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.