ABX MICROS ES 60 CT; (OPEN TUBE MODEL), (CLOSE TUBE MODEL)— 510(k) K141161

Name: FDA 510(k) clearance K141161
Creator: U.S. Food and Drug Administration
Published: 2014-12-20

Substantially Equivalent

HORIBA ABX SAS

FDA 510(k) clearance K141161 for ABX MICROS ES 60 CT; (OPEN TUBE MODEL), (CLOSE TUBE MODEL), Substantially Equivalent on 2014-12-20. Applicant: HORIBA ABX SAS. Device class: 2.

Clearance details

Applicant: HORIBA ABX SAS
Product code: Code GKZ
Device class: Class 2
Regulation: 21 CFR 864.5220
Advisory panel: Hematology
Date received: 2014-05-05
Decision date: 2014-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montpellier, FR

Download summary PDF View on FDA.gov ↗

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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.