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

Synchrony

K Number: K253473 · Decision Apr 1, 2026
Classifications
1
FEI Numbers
178
Registration Numbers
178
Same Product Code
429
Applicant Total
28
Review Days
173

Basic Information

Device Name
Synchrony
K Number
K253473
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1425
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stereotaxis, Inc.
Date Received
October 10, 2025
Decision Date
April 1, 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 Stereotaxis, Inc.

K Number Device Name
K251792 Stereotaxis GenesisX RMN with Navigant ™ Workstation (NWS)
K250590 MAGiC Sweep™ EP Mapping Catheter
K193147 Stereotaxis Genesis RMN with Navigant Workstation (NWS) and Cardiodrive System
K192775 Niobe® Magnetic Navigation System (MNS) with Navigant Workstation (NWS) and Cardiodri
K183027 Steerable catheter control system
K150312 Vdrive system, Vdrive Duo, Vdrive with V-Sono
K141530 VDRIVE SYSTEM/ VDRIVE DUO/ VDRIVE WITH V-CAS
K140804 VDRIVE WITH V-LOOP/ VDRIVE DUO
K133396 VDRIVE WITH V-SONO
K122659 VDRIVE W/V-SONO
Search all 28 clearances from Stereotaxis, Inc. →