510(k) K101776 ยท DQY Catheter, Percutaneous
SCOUTPRO ACS
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jul 23, 2010 |
| Received | Jun 25, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101776
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.