# K083413: Compurecord Peri-Operative Anesthesiology Information System

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems
- Decided: Dec 18, 2008 after 30 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: 2 generations back to K854213 (1985). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030939: Philips Compurecord Peri-Operative Information System Software, Philips Medical Systems (2003) Summary page 1.

## Indications for use
The Philips CompuRecord Peri-Operative Anesthesia Information System Software is a computer-based system which collects, processes, and records data directly from medical monitors which themselves are attached to the 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 version of the administration of anesthesia to a patient, perform a pre-operative assessment, and document (chart) nursing care in the PACU.

Source page: https://510kreport.com/device/K083413
Methodology: https://510kreport.com/methodology