# K101385: Dual Luer Lock Cap, Model 2C6250

- Pathway: 510(k) (Special)
- Applicant: Baxter Healthcare Corp
- Decided: Jun 22, 2010 after 35 days
- Product code: FPA (Set, Administration, Intravascular)
- 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: 1 generation back to K981318 (1998). 1 ancestor in all.
3 later devices descend from it; 3 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981318: Dual Luer Lock Cap, Baxter Healthcare Corp (1998) Summary page 1.

## Most influential descendants
- K200425: Female Luer Lock Cap (2020), 0 descendants of its own
- K182545: Tamper Evident Cap with Male Luer Lock (2019), 0 descendants of its own
- K140657: Curos Red Port Protector (2014), 0 descendants of its own

## Indications for use
The Dual Luer Lock Cap is indicated for use as a cap for male or female Luer ports on medical devices such as manifolds, stopcocks or sets.

Source page: https://510kreport.com/device/K101385
Methodology: https://510kreport.com/methodology