510(k) Report

510(k) · Cleared

Cleared

Power Aspirator, Model LS2 or LS2DP

K081593510(k) TraditionalCleared Jul 23, 200847-day reviewClass II21 CFR 878.5040

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

Medical Device Resource Corp. · QPB System, Suction, Lipoplasty For Removal

Cleared on Jul 23, 2008 as substantially equivalent to K854844 (Engineering, Inc., 1986) and 3 other predicates after a 47-day review. Its family tree reaches back 4 generations to 1989. 4 later devices descend from it.

Decided
Jul 23, 2008
Review
47 days
Class
Class II
Product code
QPB
Recalls
None
Predicates
4

Its longest line of descent runs back 4 generations to K895761 (1989). 6 ancestors in all, the oldest K832274 (1983). 4 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1986: 1 other ancestor1983: 1 other ancestor2009: 1 descendant cleared2017: 2 descendants cleared2015: 1 descendant clearedK895761 · General Asperator · Kolster Methods · 1989×2: 2 generations cleared close together, K980392 (1998), K981215 (1998) K032802 · HK Liposuction Aspirator, Model AP-Iii & AP230-Iii · Hk Surgical, Inc. · 200319801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 2 descendants3 generations forward: 1 descendant K032802 · HK Liposuction Aspirator, Model AP-Iii & AP230-Iii · Hk Surgical, Inc. · 2003K981215 · Psi-Tec Liposuction Aspirator · Byron Medical · 1998K980392 · Psi-Tec Aspirator · Byron Medical · 1998K895761 · General Asperator · Kolster Methods · 19890
  1. Root · 4 generations backK895761 General AsperatorKolster Methods · 1989
  2. 3 generations backK980392 Psi-Tec AspiratorByron Medical · 1998
  3. 2 generations backK981215 Psi-Tec Liposuction AspiratorByron Medical · 1998
  4. 1 generation backK032802 HK Liposuction Aspirator, Model AP-Iii & AP230-IiiHk Surgical, Inc. · 2003
  5. This deviceK081593 Power Aspirator, Model LS2 or LS2DPMedical Device Resource Corp. · 2008
  6. Descendant · cites it directly · 3 of its ownK092284 Lipisystems Aquavage, Models AV2000 and AV1200Medical Device Resource Corp. · 2009
  7. Descendant · 2 generations on · 1 of its ownK150779 LipoFilter - Hospital Pack, LipoFilter - Clinic PackMicroaire Surgical Instruments, LLC · 2015
  8. Descendant · 3 generations on · 0 of its ownK171242 Alma LipoFlow SystemAlma Lasers, Inc. · 2017
  9. Descendant · 2 generations on · 0 of its ownK161372 The Red Head Collection Device, The Jordy Connection SystemMiami Fat Supply · 2017

Most influential descendants

Showing 4 of 4 · See all
  • K092284Lipisystems Aquavage, Models AV2000 and AV1200Medical Device Resource Corp. · 2009 · cites it directly3descendants
  • K150779LipoFilter - Hospital Pack, LipoFilter - Clinic PackMicroaire Surgical Instruments, LLC · 2015 · 2 generations on1descendant
  • K171242Alma LipoFlow SystemAlma Lasers, Inc. · 2017 · 3 generations on0descendants
  • K161372The Red Head Collection Device, The Jordy Connection SystemMiami Fat Supply · 2017 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K895761General AsperatorKolster Methods1989—
−3K980392Psi-Tec AspiratorByron Medical1998—
−2K981215Psi-Tec Liposuction AspiratorByron Medical1998—
−1K032802HK Liposuction Aspirator, Model AP-Iii & AP230-IiiHk Surgical, Inc.2003—
0 (this device)K081593Power Aspirator, Model LS2 or LS2DPMedical Device Resource Corp.2008—
+1K092284Lipisystems Aquavage, Models AV2000 and AV1200Medical Device Resource Corp.2009—
+2K150779LipoFilter - Hospital Pack, LipoFilter - Clinic PackMicroaire Surgical Instruments, LLC2015—
+3K171242Alma LipoFlow SystemAlma Lasers, Inc.2017—
+2K161372The Red Head Collection Device, The Jordy Connection SystemMiami Fat Supply2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198310
198610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201510
201720
FIG. 1 — Lineage of K081593, 1989–2017Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 QPB? 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 QPB device

  1. #1 K212024 PAL Systemscore 13.7 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (4)

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
*K854844LS1000 Surgical Aspirator II
Summary page 5
…tion devices listed below in terms of intended use, design, operating principles, materials, performance, with a change of intended use: M.D. Resource: K854844 Byron Medical: K980392 Byron Medical: K98 1215 HK: K032802 6. Device Description: The LS…
Engineering, Inc.1986—
*K980392Psi-Tec Aspirator
Summary page 5
…in terms of intended use, design, operating principles, materials, performance, with a change of intended use: M.D. Resource: K854844 Byron Medical: K980392 Byron Medical: K98 1215 HK: K032802 6. Device Description: The LS Liposuction Aspirator is a power…
Byron Medical1998—
*K981215Psi-Tec Liposuction Aspirator
Summary page 5
…ign, operating principles, materials, performance, with a change of intended use: M.D. Resource: K854844 Byron Medical: K980392 Byron Medical: K98 1215 HK: K032802 6. Device Description: The LS Liposuction Aspirator is a powered suction pump! aspirator which…
Byron Medical1998—
*K032802HK Liposuction Aspirator, Model AP-Iii & AP230-Iii
Summary page 5
…les, materials, performance, with a change of intended use: M.D. Resource: K854844 Byron Medical: K980392 Byron Medical: K98 1215 HK: K032802 6. Device Description: The LS Liposuction Aspirator is a powered suction pump! aspirator which uses an electrically…
Hk Surgical, Inc.2003—

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K092284Lipisystems Aquavage, Models AV2000 and AV1200Medical Device Resource Corp.20093

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 19 years and passes through 4 companies; a new generation was cleared every 5.4 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K092284 (Medical Device Resource Corp., 2009) has gone furthest, with 3 descendants of its own.

How does its category compare?

All QPB devices

QPB System, Suction, Lipoplasty For Removal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · QPB

5so far in 2026, the most since 2007

2007: 22008: 42009: 12010: 22011: 22012: 32014: 12015: 12016: 12017: 32019: 22020: 22022: 22024: 42025: 22026 (partial year): 5
2007high 5 (2026) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QPB

194in 2024

2008: 69 days median2012: 234 days median2017: 112 days median2024: 194 days median2026 (partial year): 238 days median
2007high 238 (2026) · low 69 (2008)2026

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

Recalls per year · QPB

No recall names QPB since 2007.

Adverse event reports per year · QPB

16in 2025

2022: 52023: 282024: 162025: 16
2007high 28 (2023) · low 0 (2007)2025

MAUDE reports naming product code QPB, 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
20072—00
200846900
20091—00
20102—00
20112—00
2012323400
20130—00
20141—00
20151—00
20161—00
2017311200
20180—00
20192—00
20202—00
20210—00
20222—05
20230—028
20244194016
20252—016
202652380—

What is it indicated for?

The LS Liposuction Aspirator is for aesthetic body contouring.

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. “K081593: Power Aspirator, Model LS2 or LS2DP.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K081593

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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