# K790657: Stretcher Transit Isolater #122

- Pathway: 510(k) (Traditional)
- Applicant: Vickers America Medical Corp.
- Decided: Jul 3, 1979 after 89 days
- Product code: LGM (Chamber, Patient Isolation)
- Device class: 2
- Regulation: 21 CFR 880.5450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K052798: Capsuls, Models 2003-PUR8C, 2004-PVC8C (2006), 2 descendants of its own
- K231256: Carecube Negative Pressure Isolation Chamber (2024), 0 descendants of its own
- K163223: ORCA (tm) - Operational Rescue Containment Apparatus (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K790657
Methodology: https://510kreport.com/methodology