# K202483: MyHomeDoc

- Pathway: 510(k) (Traditional)
- Applicant: Myhomedoc, Ltd.
- Decided: Mar 23, 2021 after 207 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: 7 generations back to K952882 (1996). 39 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 41 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040178: Pulseox 5500 Finger Device, Pulseox 7500 Wristwatch Device, S.P.O. Medical Equipment, Ltd. (2004) Summary page 4.
- K160401: Tyto Stethoscope, Tyto Care, Ltd. (2016) Summary page 5.
- K163516: Braun No Touch + Forehead NTF3000 Thermometer, Kaz USA, Inc., A Helen of Troy Company (2017) Summary page 5.

## Most influential descendants
- K223785: N9+ (2023), 0 descendants of its own

## Indications for use
The MyHomeDoc device, combined with a smartphone application, is a multiple-sensor device that is intended to measure, record, and transmit the recorded data of auscultation sound of human body, human body temperature, oxygen saturation (SpO2) and pulse rate, and images of an examined body part. MyHomeDoc device is intended for use by adult lay users in a non-clinical environment. MyHomeDoc application enables counseling with the physician and transmission of the information over an IP network.

Source page: https://510kreport.com/device/K202483
Methodology: https://510kreport.com/methodology