FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

FUJIFILM Ultrasonic Endoscope EB-710US

K Number: K250863 · Decision Dec 12, 2025
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
64
Review Days
266

Basic Information

Device Name
FUJIFILM Ultrasonic Endoscope EB-710US
K Number
K250863
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fujifilm Corporation
Date Received
March 21, 2025
Decision Date
December 12, 2025
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

Similar 510(k) Clearances

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

View all

Other Clearances by Fujifilm Corporation

K Number Device Name
K253137 FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840T
K254075 Synapse Lung Nodule AI
K254189 Synapse 3D Base Tools (V7.2)
K253862 APERTO Lucent MRI System
K251861 FUJIFILM Endoscope Model ED-S100TP; FUJIFILM Endoscope Model ED-S100XP; FUJIFILM Processor Model VS-1000
K250550 FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit
K253568 Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood DH-134STR
K251386 ECHELON Synergy
K244017 FUJIFILM Endoscope Model EB-710P; FUJIFILM Processor EP-8000
K243512 FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP
Search all 64 clearances from Fujifilm Corporation →