510(k) K992703 ยท DQK Computer, Diagnostic, Programmable
CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800
| Applicant | Premier Heart, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Mar 21, 2000 |
| Received | Aug 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992703
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.