# K951127: Hewlett-Packard Model M1026A Anesthetic Gas Module

- Pathway: 510(k) (Traditional)
- Applicant: Hewlett-Packard GmbH
- Decided: Mar 24, 1995 after 11 days
- Product code: CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
446 later devices descend from it; 5 cite it directly.
0 of 447 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K982619: HP Anesthesia Gas Monitor (Watertrap), Model A02 (1998), 426 descendants of its own
- K994188: Modification to Agilent Technologies Anesthesia Gas Monitor, Model M1026A #CO5 (2000), 425 descendants of its own
- K021300: Modification of Philips Component Compact Monitor, Release a.03, Model M1275B (2002), 421 descendants of its own
- K021778: Philips Component Compact Monitor, Release a.04, Model #M1275B (2002), 407 descendants of its own
- K023871: M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70 Intellivue Patient Monitor with Portal Technology (2002), 406 descendants of its own

Source page: https://510kreport.com/device/K951127
Methodology: https://510kreport.com/methodology