RELIEEV Uterine Manipulator Injector (CUMI 5.0) (K240364)
Description
RELIEEV Uterine Manipulator Injector (CUMI 5.0) by Li Medical Corporation , Ltd., an FDA 510(k) cleared obstetrics/gynecology device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240364
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. RELIEEV Uterine Manipulator Injector (CUMI 5.0) (K240364) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K092980 | PANPAC UTERINE MANIPULATOR INJECTOR, MODEL UMI 4.5 | Panpac Medical Corporation | 2010 |
Trace the full predicate network for K240364
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.