ClearanceBrief
510(k) K081386 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

MODEL 6150 (MYLAB70) AND MODEL 6100 (MYLAB90)

ApplicantEsaote, S.p.A., Carmel IN, US
DecisionSubstantially Equivalent, Sep 25, 2008
ReceivedMay 19, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081386

DateFirm and productCodeLinked 510(k)
Jan 3, 2018ESAOTE S.P.A.
MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; PA023E Probe 7.5/10
Terminated
IYNNone listed
Jan 3, 2018ESAOTE S.P.A.
MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; Probes: BL433, C 18, CA541, EC1123, EC123, IH 618, IOT332, IOT342, L 415, LA332E, LA435, LA523, LA533, SI2C41, SL2325, TRT33
Terminated
IYNNone listed

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