510(k) K152626 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
H3+ Holter Recorder
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Feb 26, 2016 |
| Received | Sep 15, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152626
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.