510(k) Report

510(k) · Cleared

Cleared

Lsu 2000 Portable Suction Unit

K950698510(k) TraditionalCleared May 9, 199588-day reviewClass II21 CFR 878.4780

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

Laerdal Medical Corp. · JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered

Cleared on May 9, 1995 after an 88-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
May 9, 1995
Review
88 days
Class
Class II
Product code
JCX
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared1995200020052010201520202025
  1. This deviceK950698 Lsu 2000 Portable Suction UnitLaerdal Medical Corp. · 1995
  2. Descendant · cites it directly · 0 of its ownK993668 Laerdal Suction Unit,(4000) Model 78 00 20Laerdal Medical A/S · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K993668Laerdal Suction Unit,(4000) Model 78 00 20Laerdal Medical A/S · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K950698Lsu 2000 Portable Suction UnitLaerdal Medical Corp.1995—
+1K993668Laerdal Suction Unit,(4000) Model 78 00 20Laerdal Medical A/S1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K950698, 1995–1999Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JCX? 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 JCX device

  1. #1 K250964 Protable Phlegm Suction Unit (JMA D01)score 12.2 · 4 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K993668Laerdal Suction Unit,(4000) Model 78 00 20Laerdal Medical A/S19990

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?

  • Of its descendants, K993668 (Laerdal Medical A/S, 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JCX devices

JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JCX

2in 2025

2008: 42009: 12010: 12011: 22012: 22013: 52014: 42016: 22017: 22018: 22019: 32022: 12023: 12024: 12025: 22026 (partial year): 1
2007high 5 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JCX

30in 2019

2008: 43 days median2013: 144 days median2014: 106 days median2019: 30 days median
2007high 144 (2013) · low 30 (2019)2026

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

Recalls per year · JCX

1in 2020

2008: 32011: 22013: 22017: 12020: 12026 (partial year): 1
2007high 3 (2008) · low 0 (2007)2026

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

Adverse event reports per year · JCX

45in 2025

2007: 482008: 572009: 342010: 72011: 92012: 182013: 122014: 682015: 1182016: 1192017: 1022018: 1702019: 1322020: 892021: 2272022: 2152023: 1872024: 1032025: 45
2007high 227 (2021) · low 7 (2010)2025

MAUDE reports naming product code JCX, 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—048
2008443357
20091—034
20101—07
20112—29
20122—018
20135144212
20144106068
20150—0118
20162—0119
20172—1102
20182—0170
20193300132
20200—189
20210—0227
20221—0215
20231—0187
20241—0103
20252—045
20261—1—
Cite this page

510(k) Report. “K950698: Lsu 2000 Portable Suction Unit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K950698

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026