DQD — Stethoscope, Electronic Class II

FDA Device Classification

Classification Details

Product Code
DQD
Device Class
Class II
Regulation Number
870.1875
Submission Type
Review Panel
CV
Medical Specialty
Cardiovascular
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K252089tyto careTyto Stethoscope (G3)March 12, 2026
K252076kneevoiceKneevoice Cartilage Evaluation System (750-3600-001)February 6, 2026
K252284csd labseMurmur Heart AIDecember 19, 2025
K252595sparrow acousticsStethophone ProSeptember 12, 2025
K251494eko healthEko Foundation Analysis Software with Transformers (EFAST)August 12, 2025
K242971heroic faith internationalAccurSound Electronic Stethoscope (AS101)November 25, 2024
K240901sparrow acousticsStethophoneSeptember 19, 2024
K233313lapsi health holdingKeikku Electronic stethoscopeApril 10, 2024
K233609eko healthCORE 500 Digital StethoscopeMarch 28, 2024
K231551sparrow acousticsStethophoneOctober 12, 2023
K230613smartsound corporationSKEEPERAugust 2, 2023
K230823ausculthingAusculThing ACCJuly 12, 2023
K230111eko devicesCORE 500 Digital StethoscopeMay 26, 2023
K230769entac medicalPrevisEA DeviceMay 19, 2023
K223785nonagonN9+April 14, 2023
K222871sparrow acousticsStethophone v1March 29, 2023
K221805heroic faith internationalAccurSound Electronic Stethoscope AS-101March 23, 2023
K212906heartbudsHeartBuds Electronic StethoscopeMarch 14, 2023
K223166medaicaMedaica M1 Telehealth StethoscopeJanuary 19, 2023
K220466sound landibiomedi Electronic Stethoscope ES-2020November 3, 2022