510(k) K970669 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
AEROQUIP SAFESTART IV CATHETER
| Applicant | Aeroquip Medical Products, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Aug 1, 1997 |
| Received | Feb 24, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970669
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.