Stethophone— 510(k) K240901
Substantially EquivalentSparrow Acoustics, Inc.
FDA 510(k) clearance K240901 for Stethophone, Substantially Equivalent on 2024-09-19. 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lucasville, CA
Recent devices under product code DQD
view allMore clearances from Sparrow Acoustics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.