510(k) K913783 ยท DQY Catheter, Percutaneous
CORDIS PTCA GUIDING CATHETER, MODIFICATION
| Applicant | Dow Corning Wright, Arlington TN, US |
| Decision | Substantially Equivalent, Oct 18, 1991 |
| Received | Aug 14, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913783
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.