# K021941: Samplok Luer Kit

- Pathway: 510(k) (Special)
- Applicant: Itl Corporation Pty, Ltd.
- Decided: Jul 2, 2002 after 19 days
- Product code: JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection)
- Device class: 2
- Regulation: 21 CFR 862.1675
- 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 K861152 (1986). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000777: Samplok, Itl Corporation Pty, Ltd. (2000) Summary page 1.
- K992729: Nipro Luer Adaptor, Nipro Medical Corp. (2000) Summary page 1.

## Most influential descendants
- K120490: Quick Sampler Holder (2012), 0 descendants of its own

## Indications for use
The ITL SampLok® Luer Kit is intended to be used as a part of vacuum blood collection equipment for the collection of blood samples for various types of blood tests.

Source page: https://510kreport.com/device/K021941
Methodology: https://510kreport.com/methodology