# K013752: Compas as (Computerized Pulmonary Analysis System)

- Pathway: 510(k) (Traditional)
- Applicant: Morgan Scientific, Inc.
- Decided: Jan 30, 2002 after 78 days
- Product code: BZG (Spirometer, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 868.1840
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The ComPAS software is intended to operate with the ScreenStar pneumotachograph spirometer. ComPAS uses flow data from the ScreenStar to display the flow and volume information measured directly from patient effort. This information is formatted for use in pulmonary function testing and reports.

Source page: https://510kreport.com/device/K013752
Methodology: https://510kreport.com/methodology