Stethophone Pro— 510(k) K252595

Substantially Equivalent

Sparrow Acoustics, Inc.

FDA 510(k) clearance K252595 for Stethophone Pro, Substantially Equivalent on 2025-09-12. Applicant: Sparrow Acoustics, Inc.. Device class: 2.

Clearance details

Applicant: Sparrow Acoustics, Inc.
Product code: Code DQD
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 2025-08-15
Decision date: 2025-09-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Lucasville, CA

Download summary PDF View on FDA.gov ↗

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