# K043178: Grantalder Rhapsody Access Port and Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Grantadler Corportation
- Decided: Feb 2, 2006 after 443 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 K951814 (1995). 1 ancestor in all.
4 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K951814: Triumph-1 Port, Horizon Medical Products, Inc. (1995) Summary page 2.

## Most influential descendants
- K110407: Invisiport (2011), 1 descendant of its own
- K141146: Invisiport (2015), 0 descendants of its own
- K082126: Rhapsody Mri (2008), 0 descendants of its own
- K081889: Rhapsody CT (2008), 0 descendants of its own

## Indications for use
The grantAdler Rhapsody Access Port and Catheter is indicated for any patient requiring reliable repeated access of the vascular system for delivery of medications, nutritional supplementation, fluids, blood. blood products or the sampling of blood.

Source page: https://510kreport.com/device/K043178
Methodology: https://510kreport.com/methodology