HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A— 510(k) K992636

Substantially Equivalent

Hewlett-Packard Co.

FDA 510(k) clearance K992636 for HP CAREVUE 9000 CLINICAL INFORMATION SYSTEM, MODEL M2331A, Substantially Equivalent on 1999-08-31. Applicant: Hewlett-Packard Co..

Clearance details

Applicant: Hewlett-Packard Co.
Product code: Code DXJ
Advisory panel: Cardiovascular
Date received: 1999-08-06
Decision date: 1999-08-31
Decision: Substantially Equivalent
Clearance type: Special
Location: Andover, 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.