# K032018: Easy Pulse II Oxygen Conserver

- Pathway: 510(k) (Traditional)
- Applicant: Precision Medical, Inc.
- Decided: Aug 25, 2003 after 56 days
- Product code: NFB (Conserver, Oxygen)
- Device class: 2
- Regulation: 21 CFR 868.5905
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K060751: Inovo, Inc. Accupulse Single Lumen Conserving Regulator (2006), 0 descendants of its own

## Indications for use
The Precision Medical, Inc. Easy Pulse II Oxygen Conserver is intended to provide supplemental oxygen to patients who may have difficulty extracting oxygen from the air that they breathe. The patients would normally receive the oxygen via a nasal cannula. The system delivers 100% oxygen at 5 different flow settings. It is intended to be used as ambulatory source of oxygen both inside and outside of the patient’s home. It is not intended as a life supporting device. The device has no contraindications.

Source page: https://510kreport.com/device/K032018
Methodology: https://510kreport.com/methodology
