510(k) K770330 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
MONITOR, PULSE WAVE VELOCITY P607
| Applicant | Cyborg Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 24, 1977 |
| Received | Feb 17, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770330
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.