510(k) K852491 ยท DQY Catheter, Percutaneous
AMERICAN PHARMASEAL TRIPLE LUMEN CATHETER
| Applicant | American Pharmaseal Div. Ahsc, Glendale CA, US |
| Decision | Substantially Equivalent, Sep 25, 1985 |
| Received | Jun 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852491
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.