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..
Clearance details
- Applicant
- E-Med Innovations, Inc.
- Product code
- Code DQD
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.