510(k) Report

510(k) · Cleared

Cleared

Indigo Aspiration System - Modified 110 Aspiration Tubing

K180939510(k) SpecialCleared May 3, 201823-day reviewClass II21 CFR 870.5150

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

Penumbra, Inc. · QEW Peripheral Mechanical Thrombectomy With Aspiration

Cleared on May 3, 2018 as substantially equivalent to K180105 (Penumbra, Inc., 2018) after a 23-day review. Its family tree reaches back 11 generations to 2001. 21 later devices descend from it.

Decided
May 3, 2018
Review
23 days
Class
Class II
Product code
QEW
Recalls
None
Predicates
1

Its longest line of descent runs back 11 generations to K003410 (2001). 13 ancestors in all, the oldest K003086 (2001). 21 later devices descend from it, 3 citing it directly.

  1. Root · 11 generations backK003410 Concentric Retriever, Model 90030Concentric Medical, Inc. · 2001 · Recalled
  2. 7 generations between
  3. 3 generations backK160533 Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc. · 2016
  4. 2 generations backK161523 INDIGO Aspiration SystemPenumbra, Inc. · 2016
  5. 1 generation backK180105 Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration…Penumbra, Inc. · 2018
  6. This deviceK180939 Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc. · 2018
  7. Descendant · cites it directly · 14 of its ownK193244 Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc. · 2020
  8. Descendant · 2 generations on · 11 of its ownK210323 Indigo Aspiration System - Lightning Aspiration TubingPenumbra, Inc. · 2021
  9. Descendant · 3 generations on · 8 of its ownK222358 Indigo Aspiration System - Lightning FlashPenumbra, Inc. · 2022
  10. Descendant · cites it directly · 2 of its ownK234073 ICE Aspiration SystemExpanse Medical, Inc. · 2024
  11. Descendant · 4 generations on · 2 of its ownK240030 Indigo® Aspiration System - Lightning® FlashPenumbra, Inc. · 2024
Show all 11 generations
  1. Root · 11 generations backK003410 Concentric Retriever, Model 90030Concentric Medical, Inc. · 2001 · Recalled
  2. 10 generations backK030476 Modified Concentric Retriever, Model 90037Concentric Medical, Inc. · 2003 · Recalled
  3. 9 generations backK033736 Merci Retriever, Models 90065, 90066Concentric Medical, Inc. · 2004
  4. 8 generations backK072718 Penumbra SystemPenumbra, Inc. · 2007 · Recalled
  5. 7 generations backK100769 Penumbra System Separator Flex (026,032,041,054), Models PSF026…Penumbra, Inc. · 2010
  6. 6 generations backK113163 Penumbra System MaxPenumbra, Inc. · 2011
  7. 5 generations backK121917 Penumbra Embolectomy Aspiration SystemPenumbra, Inc. · 2012
  8. 4 generations backK142870 Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]Penumbra, Inc. · 2015
  9. 3 generations backK160533 Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc. · 2016
  10. 2 generations backK161523 INDIGO Aspiration SystemPenumbra, Inc. · 2016
  11. 1 generation backK180105 Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration…Penumbra, Inc. · 2018
  12. This deviceK180939 Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc. · 2018

Showing 5 of 21 descendants. See all descendants

Descendants cleared per year

2020: 32021: 12022: 12023: 12024: 52025: 52026: 5
2020high 5 (2024) · low 1 (2021)2026

Most influential descendants

Showing 5 of 21 · See all
  • K193244Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc. · 2020 · cites it directly14descendants
  • K210323Indigo Aspiration System - Lightning Aspiration TubingPenumbra, Inc. · 2021 · 2 generations on11descendants
  • K222358Indigo Aspiration System - Lightning FlashPenumbra, Inc. · 2022 · 3 generations on8descendants
  • K234073ICE Aspiration SystemExpanse Medical, Inc. · 2024 · cites it directly2descendants
  • K240030Indigo® Aspiration System - Lightning® FlashPenumbra, Inc. · 2024 · 4 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K003410Concentric Retriever, Model 90030Concentric Medical, Inc.20011
−10K030476Modified Concentric Retriever, Model 90037Concentric Medical, Inc.20032
−9K033736Merci Retriever, Models 90065, 90066Concentric Medical, Inc.2004—
−8K072718Penumbra SystemPenumbra, Inc.20071
−7K100769Penumbra System Separator Flex (026,032,041,054), Models PSF026, PSF032…Penumbra, Inc.2010—
−6K113163Penumbra System MaxPenumbra, Inc.2011—
−5K121917Penumbra Embolectomy Aspiration SystemPenumbra, Inc.2012—
−4K142870Penumbra Embolectomy Aspiration System [INDIGO Aspiration System]Penumbra, Inc.2015—
−3K160533Penumbra Embolectomy Aspiration System (INDIGOTM Aspiration System)Penumbra, Inc.2016—
−2K161523INDIGO Aspiration SystemPenumbra, Inc.2016—
−1K180105Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration System -…Penumbra, Inc.2018—
0 (this device)K180939Indigo Aspiration System - Modified 110 Aspiration TubingPenumbra, Inc.2018—
+1K193244Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc.2020—
+2K210323Indigo Aspiration System - Lightning Aspiration TubingPenumbra, Inc.2021—
+3K222358Indigo Aspiration System - Lightning FlashPenumbra, Inc.2022—
+1K234073ICE Aspiration SystemExpanse Medical, Inc.2024—
+4K240030Indigo® Aspiration System - Lightning® FlashPenumbra, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200110
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202030
202110
202210
202310
202450
202550
202650
FIG. 1 — Lineage of K180939, 2001–2026Source: 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), 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 QEW? 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 QEW device

  1. #1 K213402 Triever24, Triever20score 28.6 · 5 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
*K180105Indigo Aspiration System - Penumbra Engine Pump, Indigo Aspiration System - Penumbra…
Summary page 4
…DXE 1.6 Predicate Device 510(k) Number / Clearance Date Name of Device Name of Manufacturer Predicate Device K180105 cleared on March 8, 2018 Penumbra, Inc. Indigo Aspira…
Penumbra, Inc.2018—

What descends from it? (21)

See all 21

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

NumberDeviceApplicantDecidedDescendants
K193244Indigo Aspiration System – Lightning Aspiration TubingPenumbra, Inc.202014
K234073ICE Aspiration SystemExpanse Medical, Inc.20242
K193197QuickClear Mechanical Thrombectomy SystemVolcano Atheromed, Inc.20202

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 17 years and passes through 2 companies; a new generation was cleared every 1.5 years on median.
  • 3 of the 13 ancestors have a recall of any class.
  • Of its descendants, K193244 (Penumbra, Inc., 2020) has gone furthest, with 14 descendants of its own.

How does its category compare?

All QEW devices

QEW Peripheral Mechanical Thrombectomy With Aspiration: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · QEW

14in 2025

2008: 22009: 22012: 12013: 22014: 22015: 42016: 42017: 22018: 142019: 82020: 162021: 112022: 122023: 232024: 142025: 142026 (partial year): 10
2007high 23 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QEW

58in 2025

2015: 88 days median2016: 63 days median2018: 61 days median2019: 51 days median2020: 105 days median2021: 60 days median2022: 140 days median2023: 102 days median2024: 65 days median2025: 58 days median2026 (partial year): 74 days median
2007high 140 (2022) · low 51 (2019)2026

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

Recalls per year · QEW

7in 2022

2022: 7, 7 Class I
2007high 7 (2022) · low 0 (2007)2026

Class I (7 since 2007) Class II/III not classified

Adverse event reports per year · QEW

207in 2025

2019: 332020: 1972021: 3222022: 1252023: 1652024: 1622025: 207
2007high 322 (2021) · low 0 (2007)2025

MAUDE reports naming product code QEW, 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—00
20082—00
20092—00
20100—00
20110—00
20121—00
20132—00
20142—00
201548800
201646300
20172—00
2018146100
2019851033
2020161050197
202111600322
2022121407 (7)125
2023231020165
202414650162
202514580207
202610740—

What is it indicated for?

INDIGO Aspiration Catheters and Separators:

As part of the INDIGO Aspiration System, the INDIGO Aspiration Catheters and Separators are indicated for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems.

INDIGO Aspiration Tubing:

As part of the INDIGO Aspiration System, the INDIGO Sterile Aspiration Tubing is indicated to connect the INDIGO Aspiration Catheters to the Penumbra Aspiration Pump.

Penumbra Aspiration Pump:

The Penumbra Aspiration Pump is indicated as a vacuum source for Penumbra Aspiration Systems.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K180939: Indigo Aspiration System - Modified 110 Aspiration Tubing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K180939

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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