510(k) K901501 ยท KGC Tube, Gastro-Enterostomy
CORPAK GASTROSTOMY TUBE
| Applicant | Corpak Co., Wheeling IL, US |
| Decision | Substantially Equivalent, Jun 11, 1990 |
| Received | Mar 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901501
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.