510(k) K081603 ยท DXR Ballistocardiograph
DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300
| Applicant | Heartforce Medical, Inc., Appollo Beach FL, US |
| Decision | Substantially Equivalent, Jul 24, 2009 |
| Received | Jun 6, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081603
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.