LAP-iX Suction Irrigation

FDA 510(k) K173111 · Sejong Medical Co., Ltd.

Substantially Equivalent

510(k) numberK173111

Submission

Device name
LAP-iX Suction Irrigation
Applicant
Sejong Medical Co., Ltd.
Paju-Si, KR
Received
September 29, 2017
Decision date
November 28, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HET – Laparoscope, Gynecologic (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1720
Specialty
Obstetrics/Gynecology

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More from 270surgical , Ltd.

510(k)DeviceDecision
K253165LAP-iX2NGEI · Traditional 06/09/2026SE
K252985LaportGCJ · Traditional 05/19/2026SE
K200639LAP-iXGEI · Traditional 09/29/2021SE
K200638LAP-iX Suction IrrigationHET · Special 04/03/2020SE
K173108SmokleanFYD · Traditional 05/18/2018SE
K173112LAP-iXGEI · Traditional 11/21/2017SE
K171726LapBagGCJ · Traditional 09/25/2017SE
K171741LaportGCJ · Traditional 08/29/2017SE

Questions and answers

When was LAP-iX Suction Irrigation cleared by the FDA?

LAP-iX Suction Irrigation (K173111) received a 510(k) decision of Substantially Equivalent on November 28, 2017, 60 days after the submission was received.

What is the product code of K173111?

The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.