510(k) K052797 ยท FYD Apparatus, Exhaust, Surgical
LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM
| Applicant | Medtek Devices, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Feb 13, 2006 |
| Received | Oct 3, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052797
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.