PowerGlide Pro™ Midline Catheter (K240359)
Description
PowerGlide Pro™ Midline Catheter by Becton, Dickinson and Company (Bard Access Systems, Inc.), an FDA 510(k) cleared general hospital device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240359
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. PowerGlide Pro™ Midline Catheter (K240359) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K162377 | PowerGlide Pro Midline Catheter | C.R. Bard, Inc. | 2016 |
Trace the full predicate network for K240359
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.