510(k) K192774 ยท DQY Catheter, Percutaneous
BioCardia 8F Morph DNA Deflectable Guide Catheter
| Applicant | Biocardia, San Carlos CA, US |
| Decision | Substantially Equivalent, Jan 7, 2020 |
| Received | Sep 30, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K192774
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.