# K223480: Medipoint Blood Lancets

- Pathway: 510(k) (Traditional)
- Applicant: Medipoint Holdings, LLC
- Decided: Jan 13, 2023 after 56 days
- Product code: QRK (Single Use Only Blood Lancet Without 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
Longest line of descent: 1 generation back to K221433 (2022). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221433: Facet 28G Universal Lancet, Facet Technologies, LLC (2022) Summary page 4.
- (no number) Medipoint Blood Lancets: named in the summary without a submission number

## Indications for use
Medipoint Blood Lancets are indicated to obtain a capillary blood sample from the fingertip for testing utilizing small amounts of blood.

Source page: https://510kreport.com/device/K223480
Methodology: https://510kreport.com/methodology