CliniCloud Stethoscope— 510(k) K173448

Name: FDA 510(k) clearance K173448
Creator: U.S. Food and Drug Administration
Published: 2018-01-25

Substantially Equivalent

Stethocloud Pty.Ltd (Clinicloud)

FDA 510(k) clearance K173448 for CliniCloud Stethoscope, Substantially Equivalent on 2018-01-25. Applicant: Stethocloud Pty.Ltd (Clinicloud). Device class: 2.

Clearance details

Applicant: Stethocloud Pty.Ltd (Clinicloud)
Product code: Code DQD
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 2017-11-06
Decision date: 2018-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melbourne Vic, AU

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.