# K000777: Samplok

- Pathway: 510(k) (Traditional)
- Applicant: Itl Corporation Pty, Ltd.
- Decided: Apr 11, 2000 after 33 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K021941: Samplok Luer Kit (2002), 1 descendant of its own
- K120490: Quick Sampler Holder (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K000777
Methodology: https://510kreport.com/methodology