510(k) K120781 ยท DQY Catheter, Percutaneous
CELLO BALLOON GUIDE CATHETER (6F), 950 MM AND 1020 MM LENGTH
| Applicant | Fuji Systems Corp., San Diego CA, US |
| Decision | Substantially Equivalent, Aug 9, 2012 |
| Received | Mar 15, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120781
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.