FDA Device Intelligence
Home › Eko Devices, Inc. › CORE 500 Digital Stethoscope - Wintergreen Bundle

CORE 500 Digital Stethoscope - Wintergreen Bundle

Eko Devices, Inc. · Model E8 · UDI-DI 00850010298634

DQDDPS
1
510(k) clearances
7
Adverse events
0
Recalls
51
Facilities

Description

CORE 500 Digital Stethoscope - Wintergreen Bundle

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.