# K001803: Accelerator Reciprocating Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Byron Medical
- Decided: Aug 4, 2000 after 51 days
- Product code: QPB (System, Suction, Lipoplasty For Removal)
- Device class: 2
- Regulation: 21 CFR 878.5040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
16 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) MicroAire PAD system: named in the summary without a submission number
- (no number) Byron Medical Traditional Cannula powered by average physician: named in the summary without a submission number

## Most influential descendants
- K053451: Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction Unit), Model 00 002 252 (220 V), 00 002 318 (110 V); (2006), 13 descendants of its own
- K063336: Medela Dominant 50 Lipo, Model 600-5706 (2007), 4 descendants of its own
- K212024: PAL System (2022), 3 descendants of its own
- K150134: Basic, Dominant Flex, KV-6 (2015), 2 descendants of its own
- K072793: Liposat Basic (Infiltration Pump), Model 92-007 688 (2008), 2 descendants of its own

## Indications for use
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.

Source page: https://510kreport.com/device/K001803
Methodology: https://510kreport.com/methodology