510(k) K052767 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
AFIBALERT ATRIAL FIBRILLATION DETECTOR
| Applicant | Lechnologies Research, Inc., Sussex WI, US |
| Decision | Substantially Equivalent, Jun 23, 2006 |
| Received | Sep 30, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052767
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.