# K911191: Palco Labs Model 300 Oxygen/Pulse Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Palco Laboratories, Inc.
- Decided: Jun 10, 1991 after 84 days
- Product code: DQA (Oximeter)
- Device class: 2
- Regulation: 21 CFR 870.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K061896: Mediaid Disposable Non-Adhesive Sensors, Model CST050-2101N; Reusable Finger Clip SP02 Sensors, Model CST060-2101N (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K911191
Methodology: https://510kreport.com/methodology