# K132424: Metrixcare

- Pathway: 510(k) (Traditional)
- Applicant: The Metrix Company
- Decided: Feb 12, 2014 after 191 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) 500 ml Enteral Bag with Gravity Set (Predicate Model 51584): named in the summary without a submission number
- (no number) 1000 ml Enteral Bag with Gravity Set (Predicate Model as listed in the comparison table): named in the summary without a submission number
- (no number) 1000 ml Enteral Bag with Screw Cap & Gravity Set (Predicate Model 0009): named in the summary without a submission number
- (no number) Gravity Set with Feeding Cap (Predicate Model 0061): named in the summary without a submission number
- (no number) Gravity Set with Cross Screw Connector (Predicate Model 62552): named in the summary without a submission number

## Most influential descendants
- K170555: U Deliver Bolink ENFit Enteral Feeding Sets (2017), 3 descendants of its own
- K190310: U Deliver Bolink ENFit Enteral Feeding Sets (2019), 2 descendants of its own
- K242917: Enteral Drainage System, Enteral Medicine straw (2025), 0 descendants of its own
- K223683: EnteraLoc Flow (2023), 0 descendants of its own

## Indications for use
The device is intended to deliver liquid nutritional formulas or water to a patient's enteral access device (feeding tube).

Source page: https://510kreport.com/device/K132424
Methodology: https://510kreport.com/methodology