510(k) K901133 ยท LFJ Catheter, Subclavian
DURACATH
| Applicant | Impra, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Jun 8, 1990 |
| Received | Mar 12, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901133
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.