510(k) K062302 ยท KDQ Bottle, Collection, Vacuum
MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM
| Applicant | Millicore AB, North Attleboro MA, US |
| Decision | Substantially Equivalent, Oct 6, 2006 |
| Received | Aug 8, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062302
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.