510(k) K093510 ยท OMF Percutaneous, Implanted, Long-Term Intravascular Catheter Accessory For Catheter Position
LUMENVU CATHETER GUIDANCE SYSTEM
| Applicant | Sonosite,Inc., Philedelphia PA, US |
| Decision | Substantially Equivalent, Aug 23, 2010 |
| Received | Nov 12, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093510
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.