510(k) K072329 ยท DQY Catheter, Percutaneous
SCOUTPRO 8F, 7F AND SLITTER TOOL ADVANCED
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Mar 25, 2008 |
| Received | Aug 20, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K072329
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.