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FDA 510(k)

Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR

K-Number: K251807 · 2026-03-06

Decision Date2026-03-06
Product CodeKGE
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR is a medical device manufactured by Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2026-03-06 under approval number K251807. The device is classified under product code KGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR?

Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR is a medical device that received FDA 510(k) clearance on 2026-03-06. It is manufactured by Olympus Medical Systems Corp.. The 510(k) number is K251807.

When was Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR approved by the FDA?

Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR received FDA 510(k) clearance on 2026-03-06, under approval number K251807.

What company makes Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR?

Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR is manufactured by Olympus Medical Systems Corp..

What is the FDA product code for Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR?

The FDA product code for Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR is KGE.

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Official Source

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