510(k) K962138 ยท LNH System, Nuclear Magnetic Resonance Imaging
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| Applicant | Toshiba America Mri, Inc., S. San Francisco CA, US |
| Decision | Substantially Equivalent, Dec 23, 1996 |
| Received | Jun 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962138
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.