510(k) K885247 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR
| Applicant | Baxter Healthcare Corp, Santa Ana CA, US |
| Decision | Substantially Equivalent, Mar 10, 1989 |
| Received | Dec 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885247
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.