# K810075: Autoclix

- Pathway: 510(k) (Traditional)
- Applicant: Biodynamics Corp.
- Decided: Feb 4, 1981 after 22 days
- Product code: FMK (Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature)
- Device class: 2
- Regulation: 21 CFR 878.4850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
13 later devices descend from it; 1 cites it directly.
0 of 14 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
- K214022: Accu-Chek Softclix Blood Lancing System (2022), 12 descendants of its own
- K230712: SG Lanset I, SG Lancets, Soft Lancets (2023), 0 descendants of its own
- K230310: STAT Medical Device Lancing System (2023), 0 descendants of its own
- K222617: EasyTouch Lancing Device (2023), 0 descendants of its own
- K223815: ONE DROP Lancing Device (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K810075
Methodology: https://510kreport.com/methodology