510(k) K914030 ยท DQX Wire, Guide, Catheter
GUIDER, DASHER
| Applicant | Target Therapeutics, San Jose CA, US |
| Decision | Substantially Equivalent, Feb 11, 1992 |
| Received | Sep 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914030
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.