# K252355: K-SHIELD Advantage PORT ACCESS INFUSION SET With High Pressure Tubing

- Pathway: 510(k) (Traditional)
- Applicant: Sb-Kawasumi Laboratories, Inc.
- Decided: Nov 26, 2025 after 120 days
- Product code: PTI (Non-Coring (Huber) Needle)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K001901 (2000). 20 ancestors in all.
No later device cites it as a predicate yet.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060812: Powerport (TM)Implanted Titanium Port W/8 FR. Chronoflex Catheter-Multiple, C.R. Bard, Inc. (2006) Summary page 5.

## Indications for use
This device is an intravascular administration set with a non-coring Huber needle used for drug administration and blood sampling through implanted vascular port systems. The needle tip is equipped with an anti-needle stick protector to reduce the possibility of accidental needle sticks. This device is also applicable to high-pressure injection with power injectors, when used with a port system indicated for high-pressure injection.

Source page: https://510kreport.com/device/K252355
Methodology: https://510kreport.com/methodology