510(k) K945576 ยท EZN Dilator, Catheter, Ureteral
MEADOX SURGIMED NOPROFILE(TM) OLBERT CATHETER SYSTEM(R)
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Jan 24, 1995 |
| Received | Nov 14, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945576
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.