FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

AI-Rad Companion (Pulmonary)

K Number: K233753 · Decision Mar 21, 2024
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
31
Review Days
120

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Basic Information

Device Name
AI-Rad Companion (Pulmonary)
K Number
K233753
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Healthcare GmbH
Date Received
November 22, 2023
Decision Date
March 21, 2024
Product Code
JAK
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAK System, X-Ray, Tomography, Computed

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Other Clearances by Siemens Healthcare GmbH

K Number Device Name
K253264 myAblation Guide (VC10A)
K253689 syngo Dynamics (VA41F)
K252548 AI-Rad Companion Organs RT
K253057 AI-Rad Companion Brain MR
K252838 MAGNETOM Sola; MAGNETOM Altea; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile; MAGNETOM Vida; MAGNETOM Lumina; MAGNETOM Vida Fit; MAGNETOM Flow.Elite; MAGNETOM Flow.Neo; MAGNETOM Flow.Rise
K252608 AI-Rad Companion Prostate MR
K250443 MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile
K242551 syngo Dynamics (Version VA41D)
K242745 AI-Rad Companion Organs RT
K241770 Prostate MR AI (VA10A)
Search all 31 clearances from Siemens Healthcare GmbH →