510(k) K904410 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MEADOX(R) SURGIMED OLBERT CATH SYST/NO PROFILE(TM)
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Mar 25, 1991 |
| Received | Sep 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904410
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.