Stethophone v1— 510(k) K222871

Substantially Equivalent

Sparrow Acoustics, Inc.

FDA 510(k) clearance K222871 for Stethophone v1, Substantially Equivalent on 2023-03-29. Applicant: Sparrow Acoustics, Inc..

Clearance details

Applicant: Sparrow Acoustics, Inc.
Product code: Code DQD
Advisory panel: Cardiovascular
Date received: 2022-09-22
Decision date: 2023-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lucasville, CA

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