SERENO ELECTRONIC STETHOSCOPE— 510(k) K062481
Substantially EquivalentPishon High Tech Co., Ltd.
FDA 510(k) clearance K062481 for SERENO ELECTRONIC STETHOSCOPE, Substantially Equivalent on 2006-10-16. Applicant: Pishon High Tech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Pishon High Tech Co., Ltd.
- 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
- Deer Field, IL, US
Recent devices under product code DQD
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