# K082752: Quickpin

- Pathway: 510(k) (Traditional)
- Applicant: Laboratorios Grifols, S.A.
- Decided: Sep 29, 2008 after 10 days
- Product code: LHI (Set, I.V. Fluid Transfer)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K903493 (1991). 6 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003730: Chemo-Aide Dispensing Pin, Baxter Healthcare Corp (2000) Summary page 1.
- K040456: Fleboset Multiple, Laboratorios Grifols, S.A. (2004) Summary page 1.

## Most influential descendants
- K093182: Set Gri-Fill 3.0 (2010), 1 descendant of its own
- K102590: Fleboset Double (2011), 0 descendants of its own

## Indications for use
QUICKPIN is a Luer-lock spike used in manual or automated pharmacy compounding for addition and / or extraction of IV substances, including antineoplastics and substances for chemotherapy, from rubber-stoppered containers including multidose vials. It is equipped with a 0.2 micron hydrophobic air-filter that minimizes the formation of aerosols when preparing and dispensing the substances. This device is intended to be used by trained healthcare personnel. It is restricted to sale by or on the order of a physician.

Source page: https://510kreport.com/device/K082752
Methodology: https://510kreport.com/methodology