# K173448: CliniCloud Stethoscope

- Pathway: 510(k) (Traditional)
- Applicant: Stethocloud Pty.Ltd (Clinicloud)
- Decided: Jan 25, 2018 after 80 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: 4 generations back to K771653 (1977). 5 ancestors in all.
20 later devices descend from it; 1 cites it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050159: Modification to: 3M Littmann Electronic Stethoscope, Model 3000, 3M Company (2005) Summary page 5.

## Most influential descendants
- K181612: Tyto Stethoscope (OTC) (2018), 19 descendants of its own
- K200776: Eko CORE (2020), 13 descendants of its own
- K231551: Stethophone (2023), 2 descendants of its own
- K210736: doctorgram Stethoscope DES-I (2021), 2 descendants of its own
- K240901: Stethophone (2024), 1 descendant of its own

## Indications for use
The CliniCloud Stethoscope is a digital stethoscope intended for periodic recording of lung and heart sounds to a smartphone device, via the CliniCloud app. It is intended to be used for persons of all ages. The device is for medical diagnostics purposes only.

Source page: https://510kreport.com/device/K173448
Methodology: https://510kreport.com/methodology