510(k) K934538 ยท LNH System, Nuclear Magnetic Resonance Imaging
MRI RESONANCE DIAGNOSTIC DEVICE ACCESORY
| Applicant | Noise Cancellation Technologies, Washington DC, US |
| Decision | Substantially Equivalent, Apr 25, 1994 |
| Received | Sep 20, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934538
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.