510(k) K912890— MODEL SONICAID AXIS

Substantially Equivalent

Oxford Medilog, Inc.

Clearance details

Applicant: Oxford Medilog, Inc.
Product code: Code HGM
Advisory panel: Obstetrics/Gynecology
Date received: 1991-07-01
Decision date: 1992-01-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

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.