510(k) K921706 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
MEADOX(R) SURGIMED OLBERT CATHETER SYSTEM(R)
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, May 20, 1993 |
| Received | Apr 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921706
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.