# K032363: Zoll M Series Nibp Option

- Pathway: 510(k) (Traditional)
- Applicant: Zoll Medical Corp
- Decided: Oct 31, 2003 after 92 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K962603 (1997). 9 ancestors in all.
114 later devices descend from it; 6 cite it directly.
0 of 124 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012451: Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246, Welch Allyn Protocol, Inc. (2001)

## Most influential descendants
- K042007: Zoll E Series Defibrillator (2005), 64 descendants of its own
- K090989: Zoll R Series with Nibp and ETCO2 Options, Zoll R Series (2009), 27 descendants of its own
- K082599: Non-Invasive Continuous Blood Pressure Monitoring System Cnap Monitor 500I, 500AT (2008), 25 descendants of its own
- K151644: Masimo Root Vital Signs Monitoring System and Accessories (2016), 24 descendants of its own
- K060559: Zoll R Series Defibrillator (2006), 21 descendants of its own

## Indications for use
The ZOLL M Series NIBP Option is indicated for the noninvasive measurement of arterial blood pressure for resting patients in critical care and transport. The NIBP Option on M Series units is designed to measure blood pressure for adult, pediatric, and neonatal patients.

Source page: https://510kreport.com/device/K032363
Methodology: https://510kreport.com/methodology