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

LUMINOS Q.namix T; LUMINOS Q.namix R

K Number: K250660 · Decision Jul 14, 2025
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
15
Review Days
131

Basic Information

Device Name
LUMINOS Q.namix T; LUMINOS Q.namix R
K Number
K250660
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Medical Solutions
Date Received
March 5, 2025
Decision Date
July 14, 2025
Product Code
OWB
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
OWB Interventional Fluoroscopic X-Ray System

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