LAP-iX Suction Irrigation
FDA 510(k) K200638 · Sejong Medical Co., Ltd.
510(k) numberK200638
Submission
- Device name
- LAP-iX Suction Irrigation
- Applicant
- Sejong Medical Co., Ltd.
Paju-Si, KR - Received
- March 10, 2020
- Decision date
- April 3, 2020
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
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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| K250939 | SIRIUS Endoscope System (PR-SI-1230)HET · Traditional | Precision Robotics (Hong Kong) Limited | 08/29/2025SE |
| K243821 | i-CutHET · Traditional | A.M.I. Agency For Medical Innovations GmbH | 04/25/2025SE |
| K221642 | SIRIUS Endoscope SystemHET · Traditional | Precision Robotics (Hong Kong) Limited | 12/12/2022SE |
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| K210104 | SurroundScope SystemHET · Traditional | 270surgical , Ltd. | 07/08/2021SE |
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| K200216 | 4K UHD Camera SystemHET · Traditional | Scivita Medical Technology Co., Ltd. | 08/21/2020SE |
| K190190 | WV1 EndoscopeHET · Traditional | 270surgical , Ltd. | 11/01/2019SE |
| K190744 | Endoeye HD II (WA50040A, WA50042A, WA50050A, WA50052A)HET · Special | Olympus Winter & Ibe GmbH | 08/29/2019SE |
More from Olympus Winter & Ibe GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K253165 | LAP-iX2NGEI · Traditional | 06/09/2026SE |
| K252985 | LaportGCJ · Traditional | 05/19/2026SE |
| K200639 | LAP-iXGEI · Traditional | 09/29/2021SE |
| K173108 | SmokleanFYD · Traditional | 05/18/2018SE |
| K173111 | LAP-iX Suction IrrigationHET · Traditional | 11/28/2017SE |
| K173112 | LAP-iXGEI · Traditional | 11/21/2017SE |
| K171726 | LapBagGCJ · Traditional | 09/25/2017SE |
| K171741 | LaportGCJ · Traditional | 08/29/2017SE |
Questions and answers
When was LAP-iX Suction Irrigation cleared by the FDA?
LAP-iX Suction Irrigation (K200638) received a 510(k) decision of Substantially Equivalent on April 3, 2020, 24 days after the submission was received.
What is the product code of K200638?
The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.