# K041496: Pentatrasfu  Blood Transfusion Sets

- Pathway: 510(k) (Abbreviated)
- Applicant: Pentaferte S.P.A
- Decided: Jun 30, 2005 after 391 days
- Product code: BRZ (Set, Blood Transfusion)
- 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
Longest line of descent: 2 generations back to K924721 (1993). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023039: Blood/Solution Administration Set, Model 33.015, Tuta Healthcare Pty Limited (2002) Summary page 1.
- K924721: Baxter Solution Administration Sets, Baxter Healthcare Corp (1993) Summary page 1.

## Most influential descendants
- K083349: Blood Transfusion Set (2009), 0 descendants of its own

## Indications for use
To administer Blood and Blood Derivatives into a patient's vascular system

Source page: https://510kreport.com/device/K041496
Methodology: https://510kreport.com/methodology