510(k) K912293 ยท DQX Wire, Guide, Catheter
REMOVE LABELING RESTRICT FROM GUIDE WIRES
| Applicant | Target Therapeutics, San Jose CA, US |
| Decision | Substantially Equivalent, Dec 5, 1991 |
| Received | May 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912293
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.