# K970186: GI Supply Paracentesis Pump

- Pathway: 510(k) (Traditional)
- Applicant: Gi Supply
- Decided: Feb 14, 1997 after 28 days
- Product code: BTA (Pump, Portable, Aspiration (Manual Or Powered))
- Device class: 2
- Regulation: 21 CFR 878.4780
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K221042: Renova RP Centesis Pump (2023), 0 descendants of its own
- K161002: Aprima Smartesis Centesis Pump (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K970186
Methodology: https://510kreport.com/methodology