510(k) K923944 ยท LNH System, Nuclear Magnetic Resonance Imaging
PHILIPS GYROVIEW HR - RELEASE 2
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Apr 27, 1993 |
| Received | Aug 5, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923944
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.