510(k) K001831 ยท LHI Set, I.V. Fluid Transfer
NEEDLELESS TRANSFER DEVICE
| Applicant | Medimop Medical Projects, Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Jul 11, 2000 |
| Received | Jun 16, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001831
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.