510(k) K780812 ยท FFX System, Gastrointestinal Motility (Electrical)
ESOPHAGEAL MOTILITY SYSTEM - MODEL 3330
| Applicant | Honeywell, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 13, 1978 |
| Received | May 17, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780812
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.