510(k) Report

510(k) · Cleared

Cleared

Jobst Extremity Pump (R) System 7500

K882683510(k) TraditionalCleared Sep 20, 198882-day reviewClass II21 CFR 870.5800

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

Jobst Institute, Inc. · JOW Sleeve, Limb, Compressible

Cleared on Sep 20, 1988 after an 82-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 36 later devices descend from it.

Decided
Sep 20, 1988
Review
82 days
Class
Class II
Product code
JOW
Recalls
None
Predicates
0

36 later devices descend from it, 7 citing it directly.

Descendants, by year cleared 2013: 3 descendants cleared2008: 2 descendants cleared1996: 3 descendants cleared1997: 1 descendant cleared2001: 1 descendant cleared2012: 1 descendant cleared2011: 1 descendant cleared2010: 2 descendants cleared2016: 1 descendant cleared2020: 4 descendants cleared2009: 1 descendant cleared2017: 1 descendant cleared2015: 2 descendants cleared2025: 2 descendants cleared2024: 2 descendants cleared2018: 2 descendants cleared2023: 1 descendant cleared2021: 1 descendant cleared2026: 1 descendant cleared2019: 2 descendants cleared2022: 2 descendants cleared1990200020102020
  1. This deviceK882683 Jobst Extremity Pump (R) System 7500Jobst Institute, Inc. · 1988
  2. Descendant · cites it directly · 26 of its ownK013331 Lympha Press Plus DeviceMego Afek · 2001
  3. Descendant · 2 generations on · 17 of its ownK082149 Lympha Press Optimal, Model# 1201APMego Afek AC, Ltd. · 2008
  4. Descendant · 2 generations on · 14 of its ownK100677 Lympha Press 201MAX, Model 201MAXMego Afek AC, Ltd. · 2010
  5. Descendant · 3 generations on · 12 of its ownK123647 Circuflow 5208 Sequential Compression DeviceDevon Medical, Inc. · 2013
  6. Descendant · 2 generations on · 6 of its ownK102320 Compressible Limb and Circulation Therapy System Model LX7(V7)Daesung Maref Co., Ltd. · 2011

Showing 5 of 36 descendants. See all descendants

Descendants cleared per year

1996: 31997: 12001: 12008: 22009: 12010: 22011: 12012: 12013: 32015: 22016: 12017: 12018: 22019: 22020: 42021: 12022: 22023: 12024: 22025: 22026: 1
1996high 4 (2020) · low 0 (1998)2026

Most influential descendants

Showing 5 of 36 · See all
  • K013331Lympha Press Plus DeviceMego Afek · 2001 · cites it directly26descendants
  • K082149Lympha Press Optimal, Model# 1201APMego Afek AC, Ltd. · 2008 · 2 generations on17descendants
  • K100677Lympha Press 201MAX, Model 201MAXMego Afek AC, Ltd. · 2010 · 2 generations on14descendants
  • K123647Circuflow 5208 Sequential Compression DeviceDevon Medical, Inc. · 2013 · 3 generations on12descendants
  • K102320Compressible Limb and Circulation Therapy System Model LX7(V7)Daesung Maref Co., Ltd. · 2011 · 2 generations on6descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K882683Jobst Extremity Pump (R) System 7500Jobst Institute, Inc.1988—
+1K013331Lympha Press Plus DeviceMego Afek2001—
+2K082149Lympha Press Optimal, Model# 1201APMego Afek AC, Ltd.2008—
+2K100677Lympha Press 201MAX, Model 201MAXMego Afek AC, Ltd.2010—
+3K123647Circuflow 5208 Sequential Compression DeviceDevon Medical, Inc.2013—
+2K102320Compressible Limb and Circulation Therapy System Model LX7(V7)Daesung Maref Co., Ltd.2011—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199630
199710
200110
200820
200910
201020
201110
201210
201330
201520
201610
201710
201820
201920
202040
202110
202220
202310
202420
202520
202610
FIG. 1 — Lineage of K882683, 1988–2026Source: 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 JOW? 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 JOW device

  1. #1 K253555 Flexitouch® Plus Advanced Pneumatic…score 14.8 · 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?

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

What descends from it? (36)

See all 36

7 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K013331Lympha Press Plus DeviceMego Afek200126
K131193Actitouch Act-Adaptive Compression Therapy SystemTactile Systems Technology, Inc.20132
K971026The Circulator BootCirculator Boot Corp.19971
K071763Amadeus Adaptive Compression TherapyConvatec20080
K961891WLP Single-Segment Version WLP Solo ViiWright Linear Pump, Inc.19960
K954788Eureduc Pneumatic Drainage SystemEureduc19960
K960902Eureduc Pneumatic Drainage System Model TP03Eureduc19960

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, K013331 (Mego Afek, 2001) has gone furthest, with 26 descendants of its own.

How does its category compare?

All JOW devices

JOW Sleeve, Limb, Compressible: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JOW

7in 2025

2007: 62008: 42009: 32010: 182011: 112012: 132013: 172014: 162015: 102016: 92017: 92018: 112019: 112020: 142021: 162022: 72023: 62024: 82025: 72026 (partial year): 6
2007high 18 (2010) · low 3 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JOW

168in 2025

2007: 66 days median2008: 112 days median2009: 84 days median2010: 71 days median2011: 104 days median2012: 63 days median2013: 94 days median2014: 91 days median2015: 160 days median2016: 121 days median2017: 116 days median2018: 136 days median2019: 88 days median2020: 158 days median2021: 132 days median2022: 80 days median2023: 160 days median2024: 197 days median2025: 168 days median2026 (partial year): 252 days median
2007high 252 (2026) · low 63 (2012)2026

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

Recalls per year · JOW

1in 2019

2008: 72010: 22011: 32012: 22017: 12019: 1
2007high 7 (2008) · low 0 (2007)2026

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

Adverse event reports per year · JOW

24in 2025

2007: 122008: 362009: 452010: 662011: 502012: 1002013: 1692014: 932015: 1372016: 1502017: 1492018: 1142019: 1022020: 502021: 342022: 272023: 572024: 302025: 24
2007high 169 (2013) · low 12 (2007)2025

MAUDE reports naming product code JOW, 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
2007666012
20084112736
2009384045
20101871266
201111104350
201213632100
201317940169
20141691093
2015101600137
201691210150
201791161149
2018111360114
201911881102
202014158050
202116132034
2022780027
20236160057
20248197030
20257168024
202662520—

More from Jobst Institute, Inc.

15 FDA decisions under this applicant name. See the company

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  • K925154Jobst-CustomJobst Institute, Inc. · 1994
  • K925583Jobskin Continuing CareJobst Institute, Inc. · 1994
  • K934639Jobst Athrombic Pump - System 2500Jobst Institute, Inc. · 1994

Recent decisions in JOW

The JOW category page

  • K261807Sequential Circulator (SC-4004-DL, SC-4008-DL)Bio Compression Systems, Inc. · 2026
  • K254217AerloomEvolym, LLC · 2026
  • K253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile Medical · 2026
  • K253386DVT GarmentVistar Medical Supplies Co., Ltd. · 2026
  • K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd. · 2026

https://510kreport.com/device/K882683 · printed Nov 6, 2026

Cite this page

510(k) Report. “K882683: Jobst Extremity Pump (R) System 7500.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K882683

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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