# K170158: PowerGlide ST Midline Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Jun 1, 2017 after 134 days
- Product code: PND (Midline Catheter)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K932323 (1993). 25 ancestors in all.
No later device cites it as a predicate yet.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162377: PowerGlide Pro Midline Catheter, C.R. Bard, Inc. (2016) Summary page 4.

## Recalls of this device
- Mar 17, 2020 · Class II · Z-1946-2020: Iincorrectly packaged without the required lidocaine as labeled

## Indications for use
The PowerGlide ST Midline Catheter is inserted into a patient’s vascular system for short term use 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 ST Midline Catheter is suitable for use with power injectors.

Source page: https://510kreport.com/device/K170158
Methodology: https://510kreport.com/methodology