510(k) K944989 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
NOPROFILE OLBERT CATHETER SYSTEM
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Apr 26, 1995 |
| Received | Oct 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944989
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.