510(k) K935020 ยท MLD Monitor, St Segment With Alarm
OMNI-TRAC MODIFICATION
| Applicant | Invivo Research, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Apr 26, 1995 |
| Received | Oct 20, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935020
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.