# K974533: Trimport

- Pathway: 510(k) (Traditional)
- Applicant: Gerard Medical, Inc.
- Decided: May 7, 1998 after 156 days
- Product code: LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5965
- 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 K942623 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K942623: Trimport, Gerard Medical Enterprises, Inc. (1994) Summary page 1.

## Indications for use
Our TrimPort Systems are indicated for use whenever patient therapy requires repeated intravascular injection or continuous infusion of fluids, medications, antibiotics, nutritionals and the withdrawal of venous blood samples.

Source page: https://510kreport.com/device/K974533
Methodology: https://510kreport.com/methodology