510(k) K884806 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
LUMED EXPANDO-CATH, ACTIV
| Applicant | Luther Medical Products, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Feb 8, 1989 |
| Received | Nov 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884806
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.