510(k) K100813 ยท DPS Electrocardiograph
QRS CARD S-T SEGMENT ANALYSIS PATIENT MONITORING SYSTEM MODEL: QRS CARD USB
| Applicant | Pulse Biomedical, Inc., Norristown PA, US |
| Decision | Substantially Equivalent, Jul 23, 2010 |
| Received | Mar 23, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100813
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.