510(k) K243348

Device
Athelas Home
Applicant
Athelas, Inc.
510(k) number
K243348
Product code
GKZ
Decision
Substantially Equivalent (SESE)
Decision date
2026-02-06
Date received
2024-10-28
Regulation
864.5220
Classification name
Counter, Differential Cell
Medical specialty
Hematology
Review panel
Hematology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Tanay Tandon
Address
1300 Terra Bella Ave. Suite 200 Mountain View CA US 94043 94043

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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