# K152585: Resmon PRO FULL

- Pathway: 510(k) (Traditional)
- Applicant: Medical Graphics Corp.
- Decided: Jun 24, 2016 after 288 days
- Product code: PNV (Impedance Measuring Device Utilizing Oscillation Techniques)
- Device class: 2
- Regulation: 21 CFR 868.1840
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K954140 (1995). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101873: Masterscreen Ios, Carefusion Germany 234 GmbH (2011) Summary page 4.

## Most influential descendants
- K170185: tremoFlo C-100 Airwave Oscillometry System (2017), 1 descendant of its own
- K221024: tremoflo C2 Airwave Oscillometry System (2023), 0 descendants of its own

## Indications for use
The Resmon PRO FULL is intended to measure respiratory system impedance using the Forced Oscillation Technique (FOT). Resmon PRO FULL is intended for use with pediatric and adult patients 4 years of age or older. The device is designed to be used by pulmonologists, general practitioners, nurses, respiratory therapists, laboratory technologists, medical researchers and similarly trained personnel in hospitals, clinics, and private physician offices.

Source page: https://510kreport.com/device/K152585
Methodology: https://510kreport.com/methodology