eKuore Pro Series
K-Number: K203007 · 2020-10-30
ApplicantChip Ideas Electronics S.L.
Decision Date2020-10-30
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
eKuore Pro Series is a medical device manufactured by Chip Ideas Electronics S.L.. It received FDA 510(k) clearance on 2020-10-30 under approval number K203007. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the eKuore Pro Series?
eKuore Pro Series is a medical device that received FDA 510(k) clearance on 2020-10-30. It is manufactured by Chip Ideas Electronics S.L.. The 510(k) number is K203007.
When was eKuore Pro Series approved by the FDA?
eKuore Pro Series received FDA 510(k) clearance on 2020-10-30, under approval number K203007.
What company makes eKuore Pro Series?
eKuore Pro Series is manufactured by Chip Ideas Electronics S.L..
What is the FDA product code for eKuore Pro Series?
The FDA product code for eKuore Pro Series is DQD.
Other Devices by Chip Ideas Electronics S.L.
K181882eKuore One electronic interface for stethoscope
K201742eKuore One Wireless Electronic Interface for stethoscope
K212013eKuore Pro 4T - REF EP0098
K211779ES001 Digital stethoscope for general-purpose auscultation, ES002 Digital stethoscope for hearing impaired users, ES003 Digital stethoscope for telemedicine.
Related Devices (Code: DQD)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.