510(k) K050731 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
SEER LIGHT EXTEND COMPACT DIGITAL HOLTER SYSTEM
| Applicant | Ge Medical Systems Information Technologies, Milwaukee WI, US |
| Decision | Substantially Equivalent, May 19, 2005 |
| Received | Mar 21, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050731
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.