# K020533: Exel Vaculet Blood Collection Set

- Pathway: 510(k) (Traditional)
- Applicant: Exelint Intl. Co.
- Decided: Dec 2, 2002 after 286 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K151991: Safelock Disposable Blood Collection Set, Disposable Blood Collection Set (2015), 0 descendants of its own

## Indications for use
This device is an integral part of blood collection (intravenously) used in connection with luer adapter for collection of whole blood into tubes.

Source page: https://510kreport.com/device/K020533
Methodology: https://510kreport.com/methodology