# K150699: Bard LubriGuard Foley Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Jul 28, 2015 after 132 days
- Product code: EZL (Catheter, Retention Type, Balloon)
- Device class: 2
- Regulation: 21 CFR 876.5130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K910195 (1991). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K910195: Bard Hydrogel-Coated Foley Catheters, C.R. Bard, Inc. (1991) Summary page 4.

## Most influential descendants
- K180781: Bard Vertus Foley Catheter (2018), 0 descendants of its own

## Indications for use
The Bard LubriGuard Foley Catheter is intended for use in the drainage and/or collection and/or measurement of urine. Drainage is accomplished by inserting the catheter through the urethra and into the bladder.

Source page: https://510kreport.com/device/K150699
Methodology: https://510kreport.com/methodology