510(k) K914031 ยท DQX Wire, Guide, Catheter
GUIDER-22
| 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 K914031
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.