510(k) K870328 ยท LFJ Catheter, Subclavian
SINGLE LUMEN ACUTE CATHETER
| Applicant | Quinton, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, May 11, 1987 |
| Received | Jan 28, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870328
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.