Keikku Electronic stethoscope— 510(k) K233313
Substantially EquivalentLapsi Health Holding B.V.
FDA 510(k) clearance K233313 for Keikku Electronic stethoscope, Substantially Equivalent on 2024-04-10. Applicant: Lapsi Health Holding B.V.. Device class: 2.
Clearance details
- Applicant
- Lapsi Health Holding B.V.
- 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
- Amsterdam, NL
Recent devices under product code DQD
view allData sourced from openFDA. This site is unofficial and independent of the FDA.