# K151776: Central Venous Pressure System

- Pathway: 510(k) (Special)
- Applicant: Mespere Lifesciences, Inc.
- Decided: Aug 12, 2015 after 42 days
- Product code: PFA (Non-Invasive Central Venous Manometer)
- Device class: 2
- Regulation: 21 CFR 870.1140
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K962603 (1997). 34 ancestors in all.
No later device cites it as a predicate yet.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131085: Central Venous Pressure System - Mespere Venus 1000, Mespere Lifesciences, Inc. (2013) Summary page 4.

## Indications for use
CVP-VENUS-2000 is intended to be used by healthcare professionals for assessment of central venous blood pressure (CVP) of adult individuals.

Source page: https://510kreport.com/device/K151776
Methodology: https://510kreport.com/methodology