510(k) K042553 ยท DQY Catheter, Percutaneous
BIOCARDIA MORPH UNIVERSAL DEFLECTABLE GUIDE CATHETER
| Applicant | Biocardia, Inc., South San Francisco CA, US |
| Decision | Substantially Equivalent, Feb 17, 2005 |
| Received | Sep 20, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042553
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.