510(k) K102723 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
MODEL 950-12L HOLTER RECORDER WITHOUT ANALYSIS
| Applicant | Memtec Corp., Salem NH, US |
| Decision | Substantially Equivalent, Dec 9, 2010 |
| Received | Sep 21, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102723
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.