# K162377: PowerGlide Pro Midline Catheter

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Sep 22, 2016 after 29 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K932323 (1993). 24 ancestors in all.
4 later devices descend from it; 4 cite it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153280: PowerGlide Pro Midline Catheter, C.R. Bard, Inc. (2016) Summary page 4.

## Most influential descendants
- K252402: Midline Catheter (2025), 0 descendants of its own
- K240359: PowerGlide Pro™ Midline Catheter (2024), 0 descendants of its own
- K210047: Stiletto Extended Dwell Catheter (2021), 0 descendants of its own
- K170158: PowerGlide ST Midline Catheter (2017), 0 descendants of its own

## Indications for use
The PowerGlide Pro Midline Catheter is inserted into a patient’s vascular system for short-term use (<30 days) to sample blood or administer fluids intravenously. These catheters may be used for any patient population with consideration given to adequacy of vascular anatomy and appropriateness of the procedure. The PowerGlide Pro Midline Catheter is suitable for use with power injectors.

Source page: https://510kreport.com/device/K162377
Methodology: https://510kreport.com/methodology