# K030939: Philips Compurecord Peri-Operative Information System Software

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems
- Decided: Jul 15, 2003 after 112 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
Longest line of descent: 1 generation back to K854213 (1985). 1 ancestor in all.
8 later devices descend from it; 4 cite 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)
- K854213: Ari Standard Anesthesia Record, Agilent Technologies, Inc. (1985) Summary page 1.

## Most influential descendants
- 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
- K101439: Codonics Safe Labeling System (SLS), Model 500I/500P (2011), 1 descendant of its own

## Indications for use
The Philips CompuRecord Peri-Operative Anesthesiology Information System Software is a computer-based system which collects, processes, and records data directly from anesthesiological monitors which themselves are attached to patients in the operating room environment. CompuRecord is generally indicated in the peri-operative environment when the anesthetist decides to generate a paper and electronic record of the administration of anesthesia to a patient, perform a pre-operative assessment, and documentation of [chart] nursing care in the PACU.

Source page: https://510kreport.com/device/K030939
Methodology: https://510kreport.com/methodology