# K844008: Penlon AM1000 Anaesthesia Machine

- Pathway: 510(k) (Traditional)
- Applicant: Penlon, Inc.
- Decided: Mar 12, 1985 after 151 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K061102: Prima Anaesthesia Machine (2006), 1 descendant of its own
- K132903: Dre Ventura (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K844008
Methodology: https://510kreport.com/methodology