CliniCloud Stethoscope
K-Number: K173448 · 2018-01-25
ApplicantStethocloud Pty.Ltd (Clinicloud)
Decision Date2018-01-25
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
CliniCloud Stethoscope is a medical device manufactured by Stethocloud Pty.Ltd (Clinicloud). It received FDA 510(k) clearance on 2018-01-25 under approval 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. It is manufactured by Stethocloud Pty.Ltd (Clinicloud). The 510(k) number is K173448.
When was CliniCloud Stethoscope approved by the FDA?
CliniCloud Stethoscope received FDA 510(k) clearance on 2018-01-25, under approval number K173448.
What company makes CliniCloud Stethoscope?
CliniCloud Stethoscope is manufactured by Stethocloud Pty.Ltd (Clinicloud).
What is the FDA product code for CliniCloud Stethoscope?
The FDA product code for CliniCloud Stethoscope is DQD.
Other Devices by Stethocloud Pty.Ltd (Clinicloud)
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.