510(k) K032400 ยท FYD Apparatus, Exhaust, Surgical
LAFACI
| Applicant | Vision Pro, LLC, Washington DC, US |
| Decision | Substantially Equivalent, May 7, 2004 |
| Received | Aug 4, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032400
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.