510(k) K020634 ยท DXE Catheter, Embolectomy
MODIFICATION TO ATRIUM MEDICAL CORPORATION CLEARWAY PTFE BALLOON CATHETER
| Applicant | Atrium Medical Corp., Hudson NH, US |
| Decision | Substantially Equivalent, May 8, 2002 |
| Received | Feb 27, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020634
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.