# K854213: Ari Standard Anesthesia Record

- Pathway: 510(k) (Traditional)
- Applicant: Agilent Technologies, Inc.
- Decided: Dec 19, 1985 after 63 days
- Product code: BSZ (Gas-Machine, Anesthesia)
- Device class: 2
- Regulation: 21 CFR 868.5160
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K030939: Philips Compurecord Peri-Operative Information System Software (2003), 8 descendants of its own
- K050883: Safersleep System (2005), 6 descendants of its own
- K062388: Anesthesia Information and Digital-Drug Management System (2007), 5 descendants of its own
- K141474: Becton Dickinson Intelliport System (2014), 2 descendants of its own
- K182092: BD Intelliport System (2019), 1 descendant of its own

Source page: https://510kreport.com/device/K854213
Methodology: https://510kreport.com/methodology