510(k) K992533 ยท LNH System, Nuclear Magnetic Resonance Imaging
PHILIPS GYROSCAN INTERA (*)
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Oct 18, 1999 |
| Received | Jul 29, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992533
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.