# K972712: Core Resistant Huber Infusion Sets

- Pathway: 510(k) (Traditional)
- Applicant: Icu Medical, Inc.
- Decided: Oct 1, 1997 after 72 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) Micro Med/Core-Resistant Huber Infusion Set with and without Y-Site: named in the summary without a submission number

## Indications for use
The ICU Medical, Inc. Core Resistant Huber Infusion Set, Core Resistant Huber Infusion Set with Y Site and Core Resistant Huber Infusion Set with Y Site and CLAVE® are used to deliver solutions and drugs into vascular implant ports.

Source page: https://510kreport.com/device/K972712
Methodology: https://510kreport.com/methodology