# K232831: Quiver Aspiration Pump

- Pathway: 510(k) (Traditional)
- Applicant: Anoxia Medical, Inc.
- Decided: Feb 22, 2024 after 162 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
Longest line of descent: 1 generation back to K122756 (2012). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122756: Penumbra Pump Max (110VAC), Penumbra Pump Max (230VAC), Penumbar Pump Max Canister/Tubing, Penumbra, Inc. (2012) Summary page 5.

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

Source page: https://510kreport.com/device/K232831
Methodology: https://510kreport.com/methodology