510(k) K860441 ยท KGC Tube, Gastro-Enterostomy
ENTROKIT WITH MAGLINTE CATHETER
| Applicant | Lafayette Pharmacal, Inc., Lafayette IN, US |
| Decision | Unknown, Mar 12, 1986 |
| Received | Feb 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860441
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.