510(k) K023233 ยท BSO Catheter, Conduction, Anesthetic
EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM
| Applicant | Ebi, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Dec 13, 2002 |
| Received | Sep 27, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023233
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 15, 2003 | EBI, L.P. EBI VueCath Endoscopic Spinal System Terminated |
GWG | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.