# K011505: Immulite Intact PTH, Model LKPP1 (100 Tests), LKPP5 (500 Tests), Immulite 2000 Intact PTH, Model L2KPP (200 Tests), L2K6

- Pathway: 510(k) (Traditional)
- Applicant: Diagnostic Products Corp.
- Decided: Jul 2, 2001 after 47 days
- Product code: CEW (Radioimmunoassay, Parathyroid Hormone)
- Device class: 2
- Regulation: 21 CFR 862.1545
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K013566: Immulite Intact PTH, Immulite 2000 Intact PTH, Models LKPP1 (100 Tests), LKPP5 (500 Tests), L2KPP2 (200 Tests), L2KPP6 (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K011505
Methodology: https://510kreport.com/methodology