510(k) · Cardiovascular

Stethophone Pro

by Sparrow Acoustics, Inc.

Stethophone Pro is an AI-enabled medical device from Sparrow Acoustics, Inc. that the U.S. FDA cleared through 510(k) K252595 on September 12, 2025. Its lead review panel is Cardiovascular and its primary product code is DQD (Stethoscope, Electronic).

See also FDA-cleared AI cardiovascular devices in 2025, all FDA AI clearances in 2025, top cardiovascular AI devices.

Key facts

Submission numberK252595
Pathway510(k)
Date of final decision
Company (FDA list)Sparrow Acoustics, Inc.
Lead review panelCardiovascular
Primary product codeDQD — Stethoscope, Electronic
Applicant (openFDA)Sparrow Acoustics, Inc.
Applicant locationLucasville, CA
Device classClass 2
Regulation number21 CFR 870.1875
Decision codeSESE
Submission typeSpecial

Source: FDA AI-Enabled Medical Devices list and openFDA.

What this means

A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. Stethophone Pro went through this pathway (K252595).

openFDA lists it as a Class 2 device under 21 CFR 870.1875. Class II devices are moderate risk and are subject to general and special controls.

Product code DQD covers 14 devices on the FDA AI list. By decision date, this device is #11 of 14 under that code. Sparrow Acoustics, Inc. has 1 AI-enabled device on the list, and the Cardiovascular panel accounts for 154 in total.

Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.

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