510(k) K980980 ยท FFX System, Gastrointestinal Motility (Electrical)
MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50
| Applicant | Konigsberg Instruments, Inc., Pasadena CA, US |
| Decision | Substantially Equivalent, Jun 15, 1998 |
| Received | Mar 17, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980980
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.