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)

FDA 510(k) K252247 · Olympus Medical Systems Corporation

Substantially Equivalent

510(k) numberK252247

Submission

Device name
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
Hachioji-Shi, JP
Received
July 18, 2025
Decision date
October 16, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FBK – Endoscopic Injection Needle, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

inserted through endoscope for injection of a solution, gas, or implantable materials into gi or gu tissue.

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K232442Disposable Endoscope Injection NeedlesFBK · Traditional Zhejiang Soudon Medical Technology Co., Ltd.11/09/2023SE
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Questions and answers

When was 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) cleared by the FDA?

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) (K252247) received a 510(k) decision of Substantially Equivalent on October 16, 2025, 90 days after the submission was received.

What is the product code of K252247?

The FDA product code is FBK – Endoscopic Injection Needle, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.