PORTABLE PATIENT MONITOR— 510(k) K922974

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K922974 for PORTABLE PATIENT MONITOR, Substantially Equivalent on 1992-12-07. Applicant: Hewlett-Packard Co..

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code MHX
Advisory panel: Cardiovascular
Date received: 1992-06-22
Decision date: 1992-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MS, US

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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.