510(k) K021340 ยท DRN Device, Counter-Pulsating, External
AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE
| Applicant | External Counterpulsation Lab, Shanghai, CN |
| Decision | Substantially Equivalent, Jan 30, 2003 |
| Received | Apr 26, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021340
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.