510(k) K953608 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
NOPROFILE OLBERT CATHETER SYSTEM BALLOON DILATATION CATHETER
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Dec 20, 1995 |
| Received | Aug 2, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953608
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.