FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Definium Tempo Select

K Number: K250788 · Decision Aug 28, 2025
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
12
Review Days
167

Basic Information

Device Name
Definium Tempo Select
K Number
K250788
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Hualun Medical Systems Co. , Ltd.
Date Received
March 14, 2025
Decision Date
August 28, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KPR), ordered by most recent decision date.

View all

Other Clearances by Ge Hualun Medical Systems Co. , Ltd.

K Number Device Name
K253269 OEC One CFD
K240828 OEC One ASD
K242678 Definium Pace Select ET
K231892 Definium Pace Select
K191699 Discovery XR656 HD with VolumeRad
K182626 OEC One
K173612 Optima XR646 HD
K172700 OEC One
K172869 Discovery XR656 HD
K171800 OEC Elite MiniView
Search all 12 clearances from Ge Hualun Medical Systems Co. , Ltd. →