Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

eKuore One electronic interface for stethoscope

K-Number: K181882 · 2019-03-27

Decision Date2019-03-27
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

eKuore One electronic interface for stethoscope is a medical device manufactured by Chip Ideas Electronics S.L.. It received FDA 510(k) clearance on 2019-03-27 under approval number K181882. 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 One electronic interface for stethoscope?

eKuore One electronic interface for stethoscope is a medical device that received FDA 510(k) clearance on 2019-03-27. It is manufactured by Chip Ideas Electronics S.L.. The 510(k) number is K181882.

When was eKuore One electronic interface for stethoscope approved by the FDA?

eKuore One electronic interface for stethoscope received FDA 510(k) clearance on 2019-03-27, under approval number K181882.

What company makes eKuore One electronic interface for stethoscope?

eKuore One electronic interface for stethoscope is manufactured by Chip Ideas Electronics S.L..

What is the FDA product code for eKuore One electronic interface for stethoscope?

The FDA product code for eKuore One electronic interface for stethoscope is DQD.

Related Clinical Trials

Other Devices by Chip Ideas Electronics S.L.

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.