510(k) K112828 ยท DQY Catheter, Percutaneous
REVIVE INTERMEDIATE CATHETER (REVIVE IC)
| Applicant | Codman & Shurtleff, Inc., Raynham MA, US |
| Decision | Substantially Equivalent, Oct 25, 2011 |
| Received | Sep 28, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K112828
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.