510(k) K931896 ยท FCE Enema Kit
PRO-FLO SYSTEM
| Applicant | Lafayette Pharmacal, Inc., Lafayette IN, US |
| Decision | Substantially Equivalent, Aug 26, 1993 |
| Received | Apr 15, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K931896
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.