510(k) K252247

Device
Injector Force Max Single Use Injector (NM-400L); Injector Force Max Single Use Injector (NM-400U); Injector Force Max Single Use Injector (NM-400Y); Injector Force Max Single Use Injector (NM-401L)
Applicant
Olympus Medical Systems Corporation
510(k) number
K252247
Product code
FBK
Decision
Substantially Equivalent (SESE)
Decision date
2025-10-16
Date received
2025-07-18
Regulation
876.1500
Classification name
Endoscopic Injection Needle, Gastroenterology-Urology
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Seiko Yunoki
Address
2951 Ishikawa-Cho Hachioji-Shi JP 192-8507 192-8507

FDA Registration Numbers

Source Documents

510(k) summary PDF

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