FDA 510(k)

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

K-Nummer: K251807 · 2026-03-06

AntragstellerOlympus Medical Systems Corp.

Entscheidungsdatum2026-03-06

ProduktcodeKGE

BeratungsausschussGU

EntscheidungSubstantially Equivalent

Produktübersicht

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

Häufig gestellte Fragen

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. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K251807.

When did Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR receive FDA 510(k) clearance?

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

Who is the listed applicant for Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR?

The FDA 510(k) record lists Olympus Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

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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