# K930124: Variant of Octostop and Octopaque

- Pathway: 510(k) (Traditional)
- Applicant: Octostop, Inc.
- Decided: Feb 9, 1994 after 393 days
- Product code: KXH (Cradle, Patient, Radiologic)
- Device class: 1
- Regulation: 21 CFR 892.1830
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K122174: Pediatric Positioner Pad Set (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K930124
Methodology: https://510kreport.com/methodology