510(k) K150564 ยท DPS Electrocardiograph
Spaulding Electrocardiograph 2100iQ
| Applicant | Spaulding Clinical Research, LLC, West Bend WI, US |
| Decision | Substantially Equivalent, Aug 12, 2015 |
| Received | Mar 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150564
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.