510(k) K811629 ยท IYX Camera, Scintillation (Gamma)
DYNA- MO
| Applicant | Philips Medical Systems (Cleveland), Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 8, 1981 |
| Received | Jun 9, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811629
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.