510(k) K092253 ยท LNH System, Nuclear Magnetic Resonance Imaging
MODIFICATION TO FMRI HARDWARE SYSTEM
| Applicant | Nordicneurolab, Bergen, NO |
| Decision | Substantially Equivalent, Oct 8, 2009 |
| Received | Jul 28, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K092253
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 20, 2018 | NordicNeuroLab AS fMRI Hardware System VisualSystem allows video signals from the stimulus presentation PC to enter the shielded scanner room and presented by a set of coil-mounted displays or by an in-room LCD monit Terminated |
LNH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.