# K051758: Penumbra Aspiration Pump, Model 115V

- Pathway: 510(k) (Traditional)
- Applicant: Penumbra, Inc.
- Decided: Aug 17, 2005 after 49 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 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) Gomco Aspiration Pump, Model 405: named in the summary without a submission number

## Most influential descendants
- K173389: Rex Medical Aspiration Pump (2018), 0 descendants of its own
- K170329: Basic, Dominant Flex (2017), 0 descendants of its own
- K080745: Genadyne A4 Powered Suction Pump (2008), 0 descendants of its own

## Indications for use
The Penumbra Aspiration Pump is intended for general suction use in hospitals or clinics.

Source page: https://510kreport.com/device/K051758
Methodology: https://510kreport.com/methodology