510(k) K952887 ยท LJE Catheter, Nephrostomy
NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Aug 18, 1995 |
| Received | Jun 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952887
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.