510(k) K012141 ยท DRN Device, Counter-Pulsating, External
AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE
| Applicant | External Counterpulsation Lab, Kfar Saba, IL |
| Decision | Substantially Equivalent, Oct 25, 2001 |
| Received | Jul 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012141
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.