510(k) K123658 ยท DRX Electrode, Electrocardiograph
BIOMODULE 3-M1
| Applicant | Zephyr Technology Corporation, Stamford CT, US |
| Decision | Substantially Equivalent, Apr 24, 2013 |
| Received | Nov 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123658
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.