FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

GT300; GT300-C

K Number: K250060 · Decision Oct 8, 2025
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
24
Review Days
271

Basic Information

Device Name
GT300; GT300-C
K Number
K250060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genoray Co., Ltd.
Date Received
January 10, 2025
Decision Date
October 8, 2025
Product Code
OAS
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
OAS X-Ray, Tomography, Computed, Dental

Similar 510(k) Clearances

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

View all

Other Clearances by Genoray Co., Ltd.

K Number Device Name
K252229 BELLIGER ACE
K243420 HESTIA
K232085 DVAS (DVAS-M, DVAS-W)
K232158 GenX-CR
K230787 Oscar 15 & Oscar 15i
K220392 PAPAYA 3D & PAPAYA 3D Plus
K220423 PAPAYA & PAPAYA Plus
K211780 ZEN-2090 Turbo
K200469 PAPAYA 3D Premium & PAPAYA 3D Premium Plus
K181943 OSCAR (OSCAR Prime, OSCAR Classic)
Search all 24 clearances from Genoray Co., Ltd. →