eMurmur ID
K-Number: K181988 · 2019-04-17
Device Summary
Frequently Asked Questions
What is the eMurmur ID?
eMurmur ID is a medical device that received FDA 510(k) clearance on 2019-04-17. The listed applicant is Csd Labs GmbH. The 510(k) number is K181988.
When did eMurmur ID receive FDA 510(k) clearance?
eMurmur ID received FDA 510(k) clearance on 2019-04-17, under 510(k) number K181988.
Who is the listed applicant for eMurmur ID?
The FDA 510(k) record lists Csd Labs GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for eMurmur ID?
The FDA product code for eMurmur ID is DQD.
Other records listing Csd Labs GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DQD)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.