510(k) K972439 ยท FFX System, Gastrointestinal Motility (Electrical)
ANORECTAL MANOMETRY ANALYSIS MODULE
| Applicant | Medtronic-Synectics, Stockholm, SE |
| Decision | Substantially Equivalent, Sep 23, 1997 |
| Received | Jun 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972439
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.