GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION— 510(k) K925909

Substantially Equivalent

Alicia Diagnostics, Inc.

FDA 510(k) clearance K925909 for GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION, Substantially Equivalent on 1994-10-27. Applicant: Alicia Diagnostics, Inc..

Clearance details

Applicant: Alicia Diagnostics, Inc.
Product code: Code GKZ
Advisory panel: Hematology
Date received: 1992-11-03
Decision date: 1994-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oviedo, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GKZ

product code GKZ

Malfunction: 1,205
Total: 1,205

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.