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

Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood DH-134STR

K Number: K253568 · Decision Feb 6, 2026
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
74
Applicant Total
64
Review Days
81

Basic Information

Device Name
Hood DH-084STR; Hood DH-094STR; Hood DH-104STR; Hood DH-114STR; Hood DH-124STR; Hood DH-134STR
K Number
K253568
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fujifilm Corporation
Date Received
November 17, 2025
Decision Date
February 6, 2026
Product Code
FDS
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FDS Gastroscope And Accessories, Flexible/Rigid

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