510(k) K120964 ยท DQY Catheter, Percutaneous
UPSTREAM GR CATHETER
| Applicant | Upstream Peripheral Technologies, Philedelphia PA, US |
| Decision | Substantially Equivalent, May 25, 2012 |
| Received | Mar 30, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120964
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.