510(k) K875383 ยท KOD Catheter, Urological
LAKE CATHETER CARE KITS (MODIFICATION)
| Applicant | Lake Medical Products, Inc., St. Louis MO, US |
| Decision | Unknown, Mar 9, 1988 |
| Received | Dec 15, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875383
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.