DXH 300 COULTER CELLULAR ANALYSIS SYSTEM, DXH 300C COULTER CELLULAR ANALYSSI SYSTEM MODEL: 71772, 71771— 510(k) K100489

Name: FDA 510(k) clearance K100489
Creator: U.S. Food and Drug Administration
Published: 2010-10-26

Substantially Equivalent

Beckman Coulter Cellular

FDA 510(k) clearance K100489 for DXH 300 COULTER CELLULAR ANALYSIS SYSTEM, DXH 300C COULTER CELLULAR ANALYSSI SYSTEM MODEL: 71772, 71771, Substantially Equivalent on 2010-10-26. Applicant: Beckman Coulter Cellular. Device class: 2.

Clearance details

Applicant: Beckman Coulter Cellular
Product code: Code GKZ
Device class: Class 2
Regulation: 21 CFR 864.5220
Advisory panel: Hematology
Date received: 2010-02-19
Decision date: 2010-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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.