MODEL M1251A MON. FULL DISCLOSURE REVIEW SYSTEM— 510(k) K905788

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K905788 for MODEL M1251A MON. FULL DISCLOSURE REVIEW SYSTEM, Substantially Equivalent on 1991-06-06. Applicant: Hewlett-Packard Co..

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code DXJ
Advisory panel: Cardiovascular
Date received: 1990-12-27
Decision date: 1991-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

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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.