510(k) K930193 ยท LNH System, Nuclear Magnetic Resonance Imaging
PHILIPS ENDO-CAVITARY MRI COIL
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Jun 24, 1994 |
| Received | Jan 14, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930193
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.