510(k) K131402 ยท FYD Apparatus, Exhaust, Surgical
VISICLEAR SMOKE EVACUATION SYSTEM
| Applicant | Buffalo Filter Co., Inc., Lancaster NY, US |
| Decision | Substantially Equivalent, Mar 3, 2014 |
| Received | May 15, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131402
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.