# K172296: Stethee Pro

- Pathway: 510(k) (Traditional)
- Applicant: M3Dicine Pty, Ltd.
- Decided: Oct 30, 2017 after 91 days
- Product code: DQD (Stethoscope, Electronic)
- Device class: 2
- Regulation: 21 CFR 870.1875
- 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 K771653 (1977). 7 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083903: 3M Littmann Electronic Stethoscope, Model 3200, 3M Company (2009) Summary page 4.

## Most influential descendants
- K193631: Stethee Pro 1, Stethee Pro Software System (2020), 0 descendants of its own
- K200862: Feelix Stethoscope (2020), 0 descendants of its own

## Indications for use
The Stethee™ Pro 1 is an electronic stethoscope intended for medical diagnostic purposes only. It may be used for the detection and amplification of sounds from the heart, lungs, arteries, veins, and other internal organs. It can be used on any person undergoing a physical assessment.

Source page: https://510kreport.com/device/K172296
Methodology: https://510kreport.com/methodology