Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013445220

FEI Number

3013445220

Entity Name

ATHELAS

City/State/Country

Mountain View, CA, US

Establishment Address

1300 Terra Bella Ave, STE 200, Mountain View, CA 94043, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Athelas (Owner Number: 10053154)

Owner / Operator Contact Address

1300 Terra Bella Ave, #200, Mountain View, CA 94043, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K243348

PMA Number

N/A

All Registered Proprietary Names

Athelas One Commure One Athelas Home

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GKZ	Counter, Differential Cell	Hematology	Class 2	864.5220	2019-02-12
GKZ	Counter, Differential Cell	Hematology	Class 2	864.5220	2026-02-25

Official Correspondent

Tanay Tandon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Athelas

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K910283	Danam Electronics	DANAM DATACELL-18	1991-04-12
K102064	Becton, Dickinson & CO	BD FACS SAMPLE PREP ASSISTANT III (SPA III)	2011-03-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-05	ABX Diagnostics Inc	2	Automated Differential Cell Counter
Z-0003-05	ABX Diagnostics Inc	2	Automated Differential Cell Counter
Z-0011-2014	Siemens Healthcare Diagnostics	2	ADVIA 2120/2120i Hematology Systems with ADVIA Autoslide connected to it, SMN 10361162 and SMN 10361798 --- CLASSIFICATION NAME: Counter, Differential Cell, Automated (Particle Counter) The ADVIA 2120/2120i are hematology systems that utilizes the principles of flow cytometry in order to provide complete blood counts.
Z-0021-2013	Beckman Coulter Inc.	2	Unicel DxH 800 Coulter Cellular Analysis System, Part Number 629029. The UniCel DxH 800 Analyzer is a quantitative, automated hematology analyzer for in vitro diagnostic use in screening patient populations found in clinical laboratories. The UniCel DxH 800 Analyzer provides a: " Complete Blood Count (CBC), Leukocyte 5 Part Differential (Diff), Reticulocyte (Retic) and Nucleated Red Blood Cell (NRBC) on whole blood. " Total Nucleated Count (TNC) and Red Cell Count (RBC) on Body Fluids (cerebrospinal, serous and synovial) (BF).
Z-0033-2013	Beckman Coulter Inc.	2	CYTO-STAT tetraCHROME CD45-FITC/CD4-RD1/CD8-ECD/CD3-PC5, Part Number 6607013. Allows simultaneous identification and enumeration of total CD3+, total CD4+, total CD8+, dual CD3+/CD4+, dual CD3+/CD8+ and/or total CD3+, CD19+ and CD3+/CD56+ lymphocyte percentages and absolute counts in whole blood by flow cytometry. The systems also provide the CD4/CD8 ratio when using CD45-FITC/ CD4-RD1/CD8-ECD/CD3-PC5, and total lymphocyte percentage when using CD45-FITC/CD56-RD1/ CD19-ECD/CD3-PC5.

Similar Registrations

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3009297077	Diatron MI Plc	Budapest, HU
3027394506	Becton, Dickinson and Company, BD Biosciences	Milpitas, CA, US
2182501	R & D SYSTEMS, INC.	MINNEAPOLIS, MN, US
9613959	SYSMEX CORPORATION TECHNO PARK	KOBE Hyogo, JP
3002759288	SYSMEX CORPORATION KAKOGAWA FACTORY	Kakogawa Hyogo, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013445220. Last updated year: 2026. Please use registration number 3013445220 when referencing this establishment in official correspondence.