510(k) K240402

Device
Cito CBC System
Applicant
Cytochip, Inc.
510(k) number
K240402
Product code
GKZ
Decision
Substantially Equivalent (SESE)
Decision date
2025-02-03
Date received
2024-02-09
Regulation
864.5220
Classification name
Counter, Differential Cell
Medical specialty
Hematology
Review panel
Hematology
Device class
2
Clearance type
Dual Track
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Wendian Shi
Address
18 Technology Dr., Suite 200 Irvine CA US 92618 92618

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00850063751117CitoCBC AnalyzerCYTOCHIP INC2025-07-01

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