510(k) K093969 ยท DQY Catheter, Percutaneous
ACUITY BREAK-AWAY GUIDE CATHETER
| Applicant | Cardiac Pacemakers, Inc., St Paul MN, US |
| Decision | Substantially Equivalent, Mar 5, 2010 |
| Received | Dec 23, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093969
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.