510(k) K132068 ยท DPS Electrocardiograph
PHILIPS DXL 12/16-LEAD ECG ALGORITHM
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Sep 26, 2013 |
| Received | Jul 3, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132068
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.