510(k) K863153 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
MODIFICATION OF CARDIOINTEGRAM/CARDIOINTEGRAPH
| Applicant | Ocg Technology, Inc., Farmingdale NY, US |
| Decision | Substantially Equivalent, Jan 6, 1987 |
| Received | Aug 15, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863153
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.