# K092905: Autostart Burette

- Pathway: 510(k) (Traditional)
- Applicant: Analytica Pty, Ltd.
- Decided: Mar 4, 2010 after 164 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 K984381 (1999). 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)
- K023595: Burette-in Line (150 ML), Tuta Healthcare Pty Limited (2002) Summary page 1.

## Indications for use
Administration of fluids from a container to a patient's vascular system through a needle catheter inserted into a vein.

Source page: https://510kreport.com/device/K092905
Methodology: https://510kreport.com/methodology