510(k) K032390 ยท BSO Catheter, Conduction, Anesthetic
MODIFICATION TO EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM
| Applicant | Ebi, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Aug 29, 2003 |
| Received | Aug 4, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032390
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.