510(k) K960809 ยท LMD System, Digital Image Communications, Radiological
PHILIPS SITE VIEW WORKSTATION
| Applicant | Philips Medical Systems North America, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Apr 7, 1996 |
| Received | Feb 28, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960809
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.