# K011725: Olympus Suction Pump, Model KV-5

- Pathway: 510(k) (Traditional)
- Applicant: Keymed (Medical & Industrial Equipment), Ltd.
- Decided: Aug 31, 2001 after 88 days
- Product code: JCX (Apparatus, Suction, Ward Use, Portable, Ac-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.
8 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K130123: Basic and Dominant Flex Suction Pumps (2013), 4 descendants of its own
- K150134: Basic, Dominant Flex, KV-6 (2015), 2 descendants of its own
- K123429: Olympus Energy Power System (Eps) (2013), 1 descendant of its own
- K260892: Suction Pump (SU-90) (2026), 0 descendants of its own
- K212650: Celeris, Disposable Sinus Debrider (2022), 0 descendants of its own

## Indications for use
For aspiration during flexible endoscopy and general or surgical suction within a health care establishment. It is not intended for thoracic, domiciliary, field or transport use.

Source page: https://510kreport.com/device/K011725
Methodology: https://510kreport.com/methodology