510(k) K122247 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
LIDCORAPID V2 MONITOR
| Applicant | Lidco, Ltd., London, GB |
| Decision | Substantially Equivalent, Mar 20, 2013 |
| Received | Jul 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122247
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.