Electronic Stethoscope
K-Number: K191667 · 2019-12-18
Decision Date2019-12-18
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Electronic Stethoscope is a medical device manufactured by Hefei Mintti Medical Technology Co., Ltd. China. It received FDA 510(k) clearance on 2019-12-18 under approval number K191667. 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 Electronic Stethoscope?
Electronic Stethoscope is a medical device that received FDA 510(k) clearance on 2019-12-18. It is manufactured by Hefei Mintti Medical Technology Co., Ltd. China. The 510(k) number is K191667.
When was Electronic Stethoscope approved by the FDA?
Electronic Stethoscope received FDA 510(k) clearance on 2019-12-18, under approval number K191667.
What company makes Electronic Stethoscope?
Electronic Stethoscope is manufactured by Hefei Mintti Medical Technology Co., Ltd. China.
What is the FDA product code for Electronic Stethoscope?
The FDA product code for Electronic Stethoscope is DQD.
Related Clinical Trials
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.