SENSI— 510(k) K110704
Substantially EquivalentDiacoustic Medical Devices (Pty) , Ltd.
FDA 510(k) clearance K110704 for SENSI, Substantially Equivalent on 2011-06-24. Applicant: Diacoustic Medical Devices (Pty) , Ltd..
Clearance details
- Applicant
- Diacoustic Medical Devices (Pty) , Ltd.
- Product code
- Code DQD
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.