THE HOMMED SENTRY, MODEL 1 SENTRY— 510(k) K993938

Substantially Equivalent

Hommed, LLC

FDA 510(k) clearance K993938 for THE HOMMED SENTRY, MODEL 1 SENTRY, Substantially Equivalent on 2000-03-15. Applicant: Hommed, LLC.

Clearance details

Applicant: Hommed, LLC
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1999-11-19
Decision date: 2000-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brookfield, WI, US

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Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.