ClearanceBrief
510(k) K061916 ยท LNH System, Nuclear Magnetic Resonance Imaging

NEURO II-SE, MODELS OR-MB-DR AND OR-DR

ApplicantImris, Inc., Rockville MD, US
DecisionSubstantially Equivalent, Aug 11, 2006
ReceivedJul 6, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061916

DateFirm and productCodeLinked 510(k)
Mar 11, 2016Deerfield Imaging
Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic resonance diagnostic device (MRDD).
Terminated
LNHNone listed
Nov 21, 2012Innovative Magnetic Resonance Imaging Systems Inc.
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and Neuro III-SV Magnetic Resonance Imaging Systems.
Terminated
LNHNone listed

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