510(k) K031597 ยท IZW Collimator, Automatic, Radiographic
DUNLEE FORMAT COLLIMATOR FAMILY
| Applicant | Philips Medical Systems North America Co., Bothell WA, US |
| Decision | Substantially Equivalent, Jul 21, 2003 |
| Received | May 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031597
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.