510(k) K935512 ยท KNT Tubes, Gastrointestinal (And Accessories)
CORPAK REPLACEMENT GASTROSTOMY DEVICE STOMACORE
| Applicant | Corpak Co., Wheeling IL, US |
| Decision | Substantially Equivalent, Aug 29, 1996 |
| Received | Nov 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935512
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.