# K960490: AS/3 Compact Airway Module M-Caiov

- Pathway: 510(k) (Traditional)
- Applicant: Datex Medical Instrumentation, Inc.
- Decided: May 3, 1996 after 91 days
- Product code: CBS (Analyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.))
- Device class: 2
- Regulation: 21 CFR 868.1620
- 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. The FDA summary names its predicate without a number.
- (no number) Datex AS/3™ Airway Module G-AiOV: named in the summary without a submission number

## Indications for use
The AS/3™ Compact Airway Module M-CAiOV is intended to be used in the Datex AS/3™ Anesthesia Monitor or in the AS/3™ Compact Monitor in anesthesia department, including operation rooms (OR) and post-anesthesia care units (PACU) etc.

Source page: https://510kreport.com/device/K960490
Methodology: https://510kreport.com/methodology