ClearanceBrief
510(k) K072502 ยท DQK Computer, Diagnostic, Programmable

MODIFICATION TO: MUSE CARDIOLOGY INFORMATION SYSTEM

ApplicantGe Medical Systems Information Technologies, Wauwatosa WI, US
DecisionSubstantially Equivalent, Nov 19, 2007
ReceivedSep 6, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072502

DateFirm and productCodeLinked 510(k)
Apr 17, 2013GE Healthcare, LLC
GE Healthcare Muse v7 cardiology information system. Model number 2026443-001: MUSE 7.0 app cd, Model Number 2026443-015: MUSE 7.0.2 app cd, Model number 2026443-017: MUSE 7.1 app cd, Model number 20
Terminated
DQKNone listed
Aug 14, 2009GE Healthcare, LLC
GE Healthcare MUSE Cardiology Information Systems vs. 7.0, 7.0.1, 7.0.2, 7.1, 7.1.1. The MUSE Cardiology Information System is intended to store, access and manage cardiovascular information on adult
Terminated
DQKNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.