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

ulrichINJECT CT Motion (XD 8000)

K Number: K251295 · Decision Nov 7, 2025
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
21
Applicant Total
24
Review Days
196

Basic Information

Device Name
ulrichINJECT CT Motion (XD 8000)
K Number
K251295
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1650
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ulrich GmbH & Co. KG
Date Received
April 25, 2025
Decision Date
November 7, 2025
Product Code
IZQ
Advisory Committee
Cardiovascular
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
IZQ Injector, Contrast Medium, Automatic

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K241850 ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
K233737 ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
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