MEDICOUNT DEKA HEMATOLOGY ANALYZER— 510(k) K942525

Name: FDA 510(k) clearance K942525
Creator: U.S. Food and Drug Administration
Published: 1996-06-05

Substantially Equivalent

Cea America Corp.

FDA 510(k) clearance K942525 for MEDICOUNT DEKA HEMATOLOGY ANALYZER, Substantially Equivalent on 1996-06-05. Applicant: Cea America Corp.. Device class: 2.

Clearance details

Applicant: Cea America Corp.
Product code: Code GKZ
Device class: Class 2
Regulation: 21 CFR 864.5220
Advisory panel: Hematology
Date received: 1994-05-27
Decision date: 1996-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GKZ

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K253212 — XR-Series (XR-10, XR-20) Automated Hematology Analyzers2026-05-27
K243348 — Athelas Home2026-02-06
K251249 — Tru Hematology Test2026-01-16
K250943 — Sysmex XR-Series (XR-10) Automated Hematology Analyzer2025-06-25
K251371 — Sysmex XR-Series (XR-20) Automated Hematology Analyzer2025-06-25

More clearances from Cea America Corp.

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K834613 — WILCOR-XR RP MEDICAL FILM1984-03-05
K834614 — WILCOR-XR RP-L MEDICAL FILM1984-03-05
K834612 — WILCOR-XR RP-OG MEDICAL FILM1984-02-27
K834611 — SINGUL-XR RP NON SCREEN MED. FILM1984-02-21

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.