510(k) K834225 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
RAAF DUAL LUMEN CATH. REPAIR KIT 2.2
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 13, 1984 |
| Received | Dec 6, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K834225
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.