510(k) K833616 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
OLBERT CATHETER SYSTEM
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Walker MI, US |
| Decision | Substantially Equivalent, Dec 26, 1983 |
| Received | Oct 13, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833616
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.