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

YSIO X.pree

K Number: K250738 · Decision Jul 31, 2025
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
15
Review Days
142

Basic Information

Device Name
YSIO X.pree
K Number
K250738
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Medical Solutions
Date Received
March 11, 2025
Decision Date
July 31, 2025
Product Code
KPR
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
KPR System, X-Ray, Stationary

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