510(k) K914793 ยท KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube
MONOCRYSTANT PH/LES CATHETER, MODIFICATION
| Applicant | Synectics-Dantec, Sweden, SE |
| Decision | Substantially Equivalent, Dec 13, 1993 |
| Received | Aug 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914793
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.