510(k) K070126 ยท DQY Catheter, Percutaneous
OCCLUSION BALLOON CATHETER
| Applicant | Sentreheart, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Feb 8, 2008 |
| Received | Jan 16, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070126
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.