510(k) K083677 ยท DRX Electrode, Electrocardiograph
PHYSIOGLOVE FOR USE WITH PHYSIOGLOVE ES1
| Applicant | Commwell , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 10, 2009 |
| Received | Dec 11, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083677
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.