510(k) K924968 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
L-CATH PEEL-AWAY CATHETER SYSTEM
| Applicant | Luther Medical Products, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, May 21, 1993 |
| Received | Sep 30, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924968
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.