510(k) K882231 ยท IYE Accelerator, Linear, Medical
SL SERIES, SL 15, 18, 20 & 25 (MODIFICATION)
| Applicant | Philips Medical Systems, Inc., 5680 Da Best, NL |
| Decision | Substantially Equivalent, Sep 22, 1988 |
| Received | May 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882231
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.