Brief: Irhythm Technologies Receives FDA 510(K) Clearance For Design Updates To Its Zio® AT Device
Oct 21 (Reuters) - iRhythm Technologies Inc IRTC.O :
* IRHYTHM TECHNOLOGIES RECEIVES FDA 510(K) CLEARANCE FOR
DESIGN
UPDATES PREVIOUSLY MADE TO ITS ZIO® AT DEVICE
* ZIO AT REMAINS COMMERCIALLY AVAILABLE IN THE U.S.
Source text for Eikon: ID:nGNX66Q41m
Further company coverage: IRTC.O
((Reuters.Briefs@thomsonreuters.com;))
Recent news on iRhythm Holdings
See all newsiRhythm Holdings, Inc reports results for the quarter ended September 30 - Earnings Summary
iRhythm Q3 revenue slightly misses estimates; net loss widens YoY
Brief: iRhythm Holdings Q3 Revenue USD 221.6 Million Vs. IBES Estimate USD 222.5 Million
Brief: Irhythm Provides Update On Cybersecurity Incident Previously Disclosed In June 2026
Factbox: US companies face rise in cyber attacks