eClinic Stethopod— 510(k) K220099
Substantially EquivalentHomediagnostic, LLC
FDA 510(k) clearance K220099 for eClinic Stethopod, Substantially Equivalent on 2022-10-20. Applicant: Homediagnostic, LLC. Device class: 2.
Clearance details
- Applicant
- Homediagnostic, LLC
- 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
- Santa Clara, CA, US
Recent devices under product code DQD
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