510(k) Report

510(k) · Cleared

Cleared

LAP-iX Suction Irrigation

K200638510(k) SpecialCleared Apr 3, 202024-day reviewClass II21 CFR 884.1720

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Sejong Medical Co., Ltd. · HET Laparoscope, Gynecologic (And Accessories)

Cleared on Apr 3, 2020 as substantially equivalent to K173111 (Sejong Medical Co., Ltd., 2017) after a 24-day review. Its family tree reaches back 2 generations to 1990.

Decided
Apr 3, 2020
Review
24 days
Class
Class II
Product code
HET
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K903207 (1990). No later device cites it as a predicate yet.

  1. Root · 2 generations backK903207 Auto Suture Endoscopic Suction/Irrigatrion DeviceUnited States Surgical, A Division of Tyco Healthc · 1990
  2. 1 generation backK173111 LAP-iX Suction IrrigationSejong Medical Co., Ltd. · 2017
  3. This deviceK200638 LAP-iX Suction IrrigationSejong Medical Co., Ltd. · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K903207Auto Suture Endoscopic Suction/Irrigatrion DeviceUnited States Surgical, A Division of Tyco Healthc1990—
−1K173111LAP-iX Suction IrrigationSejong Medical Co., Ltd.2017—
0 (this device)K200638LAP-iX Suction IrrigationSejong Medical Co., Ltd.2020—
FIG. 1 — Lineage of K200638, 1990–2020Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in HET? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new HET device

  1. #1 K250939 SIRIUS Endoscope System (PR-SI-1230)score 12.9 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K173111LAP-iX Suction Irrigation
Summary page 4
…• Classification: Class II • Classification regulation: 21 CFR 884.1720 • Product Code: HET 4. Predicate Devices: LAP-iX Suction Irrigation (K173111) by Sejong Medical Co., Ltd. 5. Description: The LAP-iX Suction Irrigation provides suction or irrigation to a surg…
Sejong Medical Co., Ltd.2017—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 30 years and passes through 2 companies; a new generation was cleared every 27.2 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All HET devices

HET Laparoscope, Gynecologic (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · HET

2in 2025

2008: 32009: 12010: 12011: 22012: 22013: 22015: 22017: 22018: 12019: 22020: 22021: 42022: 12025: 2
2007high 4 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HET

269in 2021

2008: 176 days median2021: 269 days median
2007high 269 (2021) · low 176 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HET

4in 2023

2008: 42009: 12015: 12022: 12023: 4
2007high 4 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HET

4,513in 2025

2007: 1812008: 3592009: 4032010: 2142011: 4172012: 1,1182013: 1,0352014: 1752015: 1242016: 2052017: 892018: 532019: 442020: 492021: 1322022: 2162023: 8242024: 3,4962025: 4,513
2007high 4,513 (2025) · low 44 (2019)2025

MAUDE reports naming product code HET, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—0181
200831764359
20091—1403
20101—0214
20112—0417
20122—01,118
20132—01,035
20140—0175
20152—1124
20160—0205
20172—089
20181—053
20192—044
20202—049
202142690132
20221—1216
20230—4824
20240—03,496
20252—04,513
20260—0—

What is it indicated for?

The LAP-iX Suction Irrigation provides suction or irrigation to a surgical site during laparoscopic and endoscopic procedures.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K200638: LAP-iX Suction Irrigation.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200638

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026