510(k) K760886 ยท EXB Collector, Ostomy
RECTAL TUBE DEVICE
| Applicant | Van Sickle Plastics Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 9, 1976 |
| Received | Oct 22, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760886
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.