FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ZEUS Platform (FG0501US)

K Number: K252859 · Decision May 29, 2026
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
18
Review Days
262

Basic Information

Device Name
ZEUS Platform (FG0501US)
K Number
K252859
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
iRhythm Technologies, Inc.
Date Received
September 9, 2025
Decision Date
May 29, 2026
Product Code
DQK
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DQK Computer, Diagnostic, Programmable

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Other Clearances by iRhythm Technologies, Inc.

K Number Device Name
K243650 Zio® monitor (DFG0001)
K240177 Zio AT® device (A100A1001)
K240029 Zio AT® device (A100A1001)
K222389 ZEUS System
K213409 ZEUS System (Zio Watch)
K202527 Zio ECG Utilization Software (ZEUS) System
K202359 Zio Monitor
K190593 Zio XT ECG Monitoring System, Zio AT ECG Monitoring System
K181502 Zio AT ECG Monitoring System, ZEUS System
K163512 Zio AT ECG Monitoring System
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