Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR
K-Number: K251807 · 2026-03-06
Device Summary
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.
Related Clinical Trials
Other Devices by Olympus Medical Systems Corp.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.