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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Csd Labs GmbH. It received FDA 510(k) clearance on 2019-04-17 under 510(k) 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. 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.