ClearanceBrief
510(k) K004050 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

PANASONIC TELE-HOMECARE SYSTEM

ApplicantMatsushita Electric Industrial Co., Ltd., Rockville MD, US
DecisionSubstantially Equivalent, Mar 15, 2001
ReceivedDec 29, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K004050

DateFirm and productCodeLinked 510(k)
Feb 14, 2013Viterion TeleHealthcare Llc
Viterion TeleHealth Monitor Model Number V500; Product Codes 08832984 (US) and 02080468 (UK) - Physiological patient monitor (without arrhythmia detection or alarms). Viterion V100, V100-BGM and V5
Terminated
MWINone listed

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