510(k) K884337 ยท DRA Catheter, Steerable
MICRO-GUIDE SYSTEM
| Applicant | Catheter Research C/O Burditt, Bowles & Radzius, Chicago IL, US |
| Decision | Substantially Equivalent, Jan 5, 1989 |
| Received | Oct 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884337
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.