510(k) K860339 ยท DQY Catheter, Percutaneous
PERCUTANEOUS CATHETERS
| Applicant | Micor, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Mar 31, 1986 |
| Received | Jan 29, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860339
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.