# K961247: AS/3 Light Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Datex Division Instrumentarium Corp.
- Decided: Oct 23, 1996 after 205 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
511 later devices descend from it; 1 cites it directly.
0 of 512 devices 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 Compact Monitor with ESTP and NIBP modules: named in the summary without a submission number

## Most influential descendants
- K981376: Hewlett-Packard M1205A Viridia 24 CT (1999), 510 descendants of its own
- K990125: HP Viridia Component Monitoring System, Model Rev. K (1999), 509 descendants of its own
- K990972: HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP Viridia Multi-Measurement Server and Compact Portable T (1999), 462 descendants of its own
- K992273: HP Viridia Multi-Measurement Server/Compact Portable Patient Monitor M3000A/M3046A/M3016A,Rel B (2000), 451 descendants of its own
- K013199: Philips Component Compact Monitor,Model M1275B, Philips Compenent Rack, Model M1276B (2001), 431 descendants of its own

## Indications for use
AS/3 Light Monitor is intended for stationary and mobile indoor monitoring of a patient’s vital signs.

Source page: https://510kreport.com/device/K961247
Methodology: https://510kreport.com/methodology