# K141200: Padi-Lock

- Pathway: 510(k) (Traditional)
- Applicant: Padi-Lock, LLC
- Decided: Oct 2, 2014 after 146 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: 2 generations back to K003225 (2000). 2 ancestors in all.
No later device cites it as a predicate yet.
1 of 3 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112893: Clearlink Luer Activated Valve, Clearlink System Non-Dehp Catheter Extension Sets, Baxter Healthcare Corporation (2011) Summary page 4.

## Indications for use
For use with a vascular access device for the administration of drugs and solutions. The Padi-Lock Medical Tubing Length Reducing Apparatus can be connected to the administration set by snaking the excess tubing through the device to shorten the length of the tubing. The device is intended to be used in hospitals and home patient care where IV tubing is used.

Source page: https://510kreport.com/device/K141200
Methodology: https://510kreport.com/methodology