510(k) K000832 ยท LNH System, Nuclear Magnetic Resonance Imaging
STEROTACTIC LOCALIZATION DEVICE (SLD)
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Apr 27, 2000 |
| Received | Mar 14, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000832
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.