DeviceClearance

CORE 500 Digital Stethoscope— 510(k) K233609

Substantially Equivalent

Eko Health, Inc.

FDA 510(k) clearance K233609 for CORE 500 Digital Stethoscope, Substantially Equivalent on 2024-03-28. Applicant: Eko Health, Inc..

Clearance details

Applicant
Eko Health, Inc.
Product code
Code DQD
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Emeryville, CA, US
Download summary PDFView on FDA.gov ↗

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