510(k) K101282 ยท DQY Catheter, Percutaneous
SCOUTPRO HEMOSTATIC VALVE
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jul 21, 2010 |
| Received | May 6, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101282
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.