Automated ankle brachial pressure index measuring device, MESI mTABLET system— 510(k) K201046
Substantially EquivalentMesi D.O.O.; Mesi, Development of Medical Devices, Ltd.
FDA 510(k) clearance K201046 for Automated ankle brachial pressure index measuring device, MESI mTABLET system, Substantially Equivalent on 2020-12-11. Applicant: Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd..
Clearance details
- Applicant
- Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd.
- Product code
- Code JOM
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ljubljana, SI
Data sourced from openFDA. This site is unofficial and independent of the FDA.