510(k) K972121 ยท MLD Monitor, St Segment With Alarm
ACUITY CENTRAL STATION
| Applicant | Protocol Systems, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Nov 7, 1997 |
| Received | Jun 5, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972121
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.