510(k) K970644 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
AEROQUIP SAFESTART (TM) IV CATH (TM) SYSTEM
| Applicant | Aeroquip Medical Products, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Jul 31, 1997 |
| Received | Feb 20, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970644
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.