510(k) K760523— MONITOR SCOPE

Substantially Equivalent

Hewlett-Packard Co.

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code DXJ
Advisory panel: Cardiovascular
Date received: 1976-08-26
Decision date: 1976-09-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Adverse events under product code DXJ

product code DXJ

Death: 2
Total: 2

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.