eMurmur ID
K-Number: K181988 · 2019-04-17
ApplicantCsd Labs GmbH
Decision Date2019-04-17
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
eMurmur ID is a medical device manufactured by Csd Labs GmbH. It received FDA 510(k) clearance on 2019-04-17 under approval number K181988. 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 eMurmur ID?
eMurmur ID is a medical device that received FDA 510(k) clearance on 2019-04-17. It is manufactured by Csd Labs GmbH. The 510(k) number is K181988.
When was eMurmur ID approved by the FDA?
eMurmur ID received FDA 510(k) clearance on 2019-04-17, under approval number K181988.
What company makes eMurmur ID?
eMurmur ID is manufactured by Csd Labs GmbH.
What is the FDA product code for eMurmur ID?
The FDA product code for eMurmur ID is DQD.
Other Devices by Csd Labs GmbH
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.