510(k) K903216 ยท DQY Catheter, Percutaneous
THE GUIDER CORONARY GUIDING CATHETER
| Applicant | Intec Medical, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Oct 19, 1990 |
| Received | Jul 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903216
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.