510(k) K962918 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
LIDCO SYSTEM
| Applicant | Lidco, Ltd., Rockville MD, US |
| Decision | Substantially Equivalent, Jan 8, 1999 |
| Received | Jun 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962918
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.