HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANCE AND ARCHIVING SYSTEM— 510(k) K970456

Substantially Equivalent

Hewlett-Packard GmbH

FDA 510(k) clearance K970456 for HEWLETT APCKARD SERIES 50 OB TRACEVUE OBSTETRICAL SURVEILLANCE AND ARCHIVING SYSTEM, Substantially Equivalent on 1997-10-03. Applicant: Hewlett-Packard GmbH.

Clearance details

Applicant: Hewlett-Packard GmbH
Product code: Code HGM
Advisory panel: Obstetrics/Gynecology
Date received: 1997-02-06
Decision date: 1997-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wuerttemberg, DE

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Adverse events under product code HGM

product code HGM

Death: 35
Malfunction: 478
Total: 513

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.