510(k) · Cleared
ClearedAccelerator Reciprocating Cannula
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Byron Medical · QPB System, Suction, Lipoplasty For Removal
Cleared on Aug 4, 2000 after a 51-day review. The FDA summary names its predicate without a number. 16 later devices descend from it.
- Decided
- Aug 4, 2000
- Review
- 51 days
- Class
- Class II
- Product code
- QPB
- Recalls
- None
- Predicates
- 0
16 later devices descend from it, 2 citing it directly.
- This deviceK001803 Accelerator Reciprocating CannulaByron Medical · 2000
- Descendant · cites it directly · 13 of its ownK053451 Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction…Moeller Medical GmbH & Co. KG · 2006
- Descendant · 2 generations on · 4 of its ownK063336 Medela Dominant 50 Lipo, Model 600-5706Medela AG · 2007
- Descendant · 2 generations on · 3 of its ownK212024 PAL SystemMicroaire Surgical Instruments, LLC · 2022
- Descendant · 3 generations on · 2 of its ownK150134 Basic, Dominant Flex, KV-6Medela AG · 2015
- Descendant · 2 generations on · 2 of its ownK072793 Liposat Basic (Infiltration Pump), Model 92-007 688Moeller Medical GmbH & Co. KG · 2008
Showing 5 of 16 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 16 · See all- K053451Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction Unit), Model 00 002 252…Moeller Medical GmbH & Co. KG · 2006 · cites it directly13descendants
- K063336Medela Dominant 50 Lipo, Model 600-5706Medela AG · 2007 · 2 generations on4descendants
- K212024PAL SystemMicroaire Surgical Instruments, LLC · 2022 · 2 generations on3descendants
- K150134Basic, Dominant Flex, KV-6Medela AG · 2015 · 3 generations on2descendants
- K072793Liposat Basic (Infiltration Pump), Model 92-007 688Moeller Medical GmbH & Co. KG · 2008 · 2 generations on2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K001803 | Accelerator Reciprocating Cannula | Byron Medical | 2000 | — |
| +1 | K053451 | Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction Unit), Model… | Moeller Medical GmbH & Co. KG | 2006 | — |
| +2 | K063336 | Medela Dominant 50 Lipo, Model 600-5706 | Medela AG | 2007 | — |
| +2 | K212024 | PAL System | Microaire Surgical Instruments, LLC | 2022 | — |
| +3 | K150134 | Basic, Dominant Flex, KV-6 | Medela AG | 2015 | — |
| +2 | K072793 | Liposat Basic (Infiltration Pump), Model 92-007 688 | Moeller Medical GmbH & Co. KG | 2008 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2001 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2008 | 2 | 0 |
| 2015 | 1 | 0 |
| 2017 | 3 | 0 |
| 2022 | 2 | 0 |
| 2024 | 2 | 0 |
| 2026 | 3 | 0 |
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 K212024 PAL Systemscore 13.7 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | MicroAire PAD system Named without a submission number | |
| * | — | Byron Medical Traditional Cannula powered by average physician Named without a submission number |
What descends from it? (16)
See all 162 later devices cite it directly; ranked here by how many devices descend from each in turn.
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, K053451 (Moeller Medical GmbH & Co. KG, 2006) has gone furthest, with 13 descendants of its own.
How does its category compare?
All QPB devicesQPB System, Suction, Lipoplasty For Removal: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · QPB
5so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · QPB
194in 2024
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
MAUDE reports naming product code QPB, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 2 | — | 0 | 0 |
| 2008 | 4 | 69 | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 2 | — | 0 | 0 |
| 2011 | 2 | — | 0 | 0 |
| 2012 | 3 | 234 | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 1 | — | 0 | 0 |
| 2016 | 1 | — | 0 | 0 |
| 2017 | 3 | 112 | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 2 | — | 0 | 0 |
| 2020 | 2 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 2 | — | 0 | 5 |
| 2023 | 0 | — | 0 | 28 |
| 2024 | 4 | 194 | 0 | 16 |
| 2025 | 2 | — | 0 | 16 |
| 2026 | 5 | 238 | 0 | — |
What is it indicated for?
The Accelerator Reciprocating Cannula indications for use are the removal of tissue or fluid from the body during general surgical procedures including suction lipoplasty for the purpose of aesthetic body contouring.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K001803 · printed Nov 6, 2026
Cite this page
510(k) Report. “K001803: Accelerator Reciprocating Cannula.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K001803
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026