GENESIS HEALTH RECORD SYSTEM, (GHRS)— 510(k) K123136

Substantially Equivalent

Genesis Health Technologies

FDA 510(k) clearance K123136 for GENESIS HEALTH RECORD SYSTEM, (GHRS), Substantially Equivalent on 2013-03-07. Applicant: Genesis Health Technologies.

Clearance details

Applicant: Genesis Health Technologies
Product code: Code NBW
Advisory panel: Clinical Chemistry
Date received: 2012-10-05
Decision date: 2013-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfield, IA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NBW

product code NBW

Death: 18
Injury: 4,740
Malfunction: 42,679
Other: 6
Total: 47,443

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.