ClearanceBrief
510(k) K992340 ยท DQA Oximeter

MASIMO SET RADICAL PULSE OXIMETER WITH SATSHARE, MASIMO LNOP -ADT-ADULT/PEDIATRIC DISPOSABLE SENSOR, MASIMO LNOP -PDT-PE

ApplicantMasimo Corp., Irvine CA, US
DecisionSubstantially Equivalent, Oct 8, 1999
ReceivedJul 13, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992340

DateFirm and productCodeLinked 510(k)
Jun 25, 2005Masimo Corporation
Radical Handheld Pulse Oximeter
Terminated
DQANone listed

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