510(k) K151135 ยท DPS Electrocardiograph
MODEL 621/624 BIOMAGNETOMETER
| Applicant | Tristan Technologies, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Mar 15, 2016 |
| Received | Apr 29, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151135
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.