E-STETH ELECTRONIC STETHOSCOPE— 510(k) K011898
Substantially EquivalentE-Med Innovations, Inc.
FDA 510(k) clearance K011898 for E-STETH ELECTRONIC STETHOSCOPE, Substantially Equivalent on 2001-09-14. Applicant: E-Med Innovations, Inc.. Device class: 2.
Clearance details
- Applicant
- E-Med Innovations, 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
- Dallas, TX, US
Recent devices under product code DQD
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