510(k) K063363 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
FIRMGRIP PERIPHERALLY INSERTED CATHETER DEVICE
| Applicant | Flexicath , Ltd., Kfar Saba, IL |
| Decision | Substantially Equivalent, May 7, 2007 |
| Received | Nov 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063363
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.