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FDA 510(k)

CliniCloud Stethoscope

K-Number: K173448 · 2018-01-25

Decision Date2018-01-25
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CliniCloud Stethoscope is the device name listed in this FDA 510(k) record. The listed applicant is Stethocloud Pty.Ltd (Clinicloud). It received FDA 510(k) clearance on 2018-01-25 under 510(k) number K173448. 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 CliniCloud Stethoscope?

CliniCloud Stethoscope is a medical device that received FDA 510(k) clearance on 2018-01-25. The listed applicant is Stethocloud Pty.Ltd (Clinicloud). The 510(k) number is K173448.

When did CliniCloud Stethoscope receive FDA 510(k) clearance?

CliniCloud Stethoscope received FDA 510(k) clearance on 2018-01-25, under 510(k) number K173448.

Who is the listed applicant for CliniCloud Stethoscope?

The FDA 510(k) record lists Stethocloud Pty.Ltd (Clinicloud) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CliniCloud Stethoscope?

The FDA product code for CliniCloud Stethoscope is DQD.

Other records listing Stethocloud Pty.Ltd (Clinicloud) 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.