510(k) K881772 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
SENSOCOR(TM) R-TEST 240 XL
| Applicant | Sensormedix, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Nov 9, 1988 |
| Received | Apr 26, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881772
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.