# K191689: EleGARD Patient Positioning System

- Pathway: 510(k) (Traditional)
- Applicant: Minnesota Resuscitation Solutions, D.B.D Advancedcpr Solutio
- Decided: Feb 13, 2020 after 233 days
- Product code: FOA (Board, Cardiopulmonary)
- Device class: 1
- Regulation: 21 CFR 880.6080
- 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. The FDA summary names its predicate without a number.
- (no number) Heads Up Platform: named in the summary without a submission number

## Most influential descendants
- K221901: EleGARD (2022), 0 descendants of its own

## Indications for use
The EleGARD™ Patient Positioning System is cardiopulmonary board which may elevate a patient’s head and thorax including during airway management; during manual CPR, manual CPR adjuncts, CPR with the LUCAS Chest Compression Systems; and patient transport.

Source page: https://510kreport.com/device/K191689
Methodology: https://510kreport.com/methodology