# K832520: Suction Tips

- Pathway: 510(k) (Traditional)
- Applicant: Wells Johnson Co.
- Decided: Oct 20, 1983 after 73 days
- Product code: GEA (Cannula, Surgical, General & Plastic Surgery)
- Device class: 1
- Regulation: 21 CFR 878.4800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 5 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K973268: Microaire Power Aspiration Device Pad System (1997), 4 descendants of its own
- K984363: XPS Tissue Aspiration System, XPS Straightshot or Model 2000 Microdebrider System (1999), 3 descendants of its own
- K040239: Supraflow Console (2004), 2 descendants of its own
- K992855: XPS Straightshot or Model 2000 Microdebrider System or XPS Powersculpt (2000), 2 descendants of its own
- K080845: Orwell Fluid Collection and Disposal System (2008), 1 descendant of its own

Source page: https://510kreport.com/device/K832520
Methodology: https://510kreport.com/methodology