510(k) K091600 ยท FGC Urethroscope
DIRECTVISION GUIDE SYSTEM
| Applicant | Percuvision, LLC, Gahanna OH, US |
| Decision | Substantially Equivalent, Aug 25, 2009 |
| Received | Jun 3, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091600
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.