510(k) K820444 ยท KHX Platform, Force-Measuring
HEART-ALERT
| Applicant | Medical Equipment Devices, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 12, 1982 |
| Received | Feb 18, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820444
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.