14 devices · 13 companies · 2012 to 2026

Product code DQD: Stethoscope, Electronic

14 devices under product code DQD, 2012 to 2026, from 13 companies. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (14 of 14 here), the regulation, and MAUDE report counts by product code.

Stethoscope, Electronic. 21 CFR 870.1875, Class II. MAUDE held 7 adverse-event reports against this product code as of 2026-10-29; reports are unverified and the code is shared by every device of this type.

Retrieved from FDA public records.

Companies with more than one device here

Every device, newest decision first

DQD · 14 devices
DecisionDeviceCompanyPanelFDA
Tyto StethoscopeK252089 · 510(k)Tyto Care , Ltd.Cardiovasculardatabase entry
Kneevoice Cartilage Evaluation SystemK252076 · 510(k)Kneevoice, Inc.Cardiovasculardatabase entry
eMurmur Heart AIK252284 · 510(k)Csd LabsCardiovasculardatabase entry
Stethophone ProK252595 · 510(k)Sparrow Acoustics, Inc.Cardiovasculardatabase entry
Eko Foundation Analysis Software with TransformeK251494 · 510(k)Eko Health, Inc.Cardiovasculardatabase entry
AusculThing ACCK230823 · 510(k)AusculThing OyCardiovasculardatabase entry
Eko Murmur Analysis SoftwareK213794 · 510(k)Eko Devices, Inc.Cardiovasculardatabase entry
eMurmur Heart AIK220766 · 510(k)CSD Labs GmbHCardiovasculardatabase entry
Stethee Pro 1, Stethee Pro Software SystemK193631 · 510(k)M3DICINE Pty Ltd.Cardiovasculardatabase entry
eMurmur IDK181988 · 510(k)CSD Labs GmbHCardiovasculardatabase entry
Tyto StethoscopeK160401 · 510(k)Tyto Care Ltd.Cardiovasculardatabase entry
Steth IOK160016 · 510(k)STRATOSCIENTIFIC, INC.Cardiovasculardatabase entry
SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICK131044 · 510(k)DIACOUSTIC MEDICAL DEVICES (PTY) LTD.Cardiovasculardatabase entry
SENSICARDIACK121617 · 510(k)DIACOUSTIC MEDICAL (PTY)Cardiovasculardatabase entry

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