510(k) K980937 ยท DRN Device, Counter-Pulsating, External
NICORE MODEL ESP -1
| Applicant | Nicore Equipment & Leasing, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Sep 15, 2000 |
| Received | Mar 12, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980937
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.