ZORTRAN DETECTOR— 510(k) K000997

Substantially Equivalent

Lucent Medical Systems

FDA 510(k) clearance K000997 for ZORTRAN DETECTOR, Substantially Equivalent on 2000-09-07. Applicant: Lucent Medical Systems.

Clearance details

Applicant: Lucent Medical Systems
Product code: Code FOZ
Advisory panel: General Hospital
Date received: 2000-03-28
Decision date: 2000-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kirkland, WA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.