# K850959: Equipment Snap Kovers

- Pathway: 510(k) (Traditional)
- Applicant: Advance Medical Designs, Inc.
- Decided: Apr 9, 1985 after 32 days
- Product code: JAA (System, X-Ray, Fluoroscopic, Image-Intensified)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: 1 (0 Class I)
- 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
- K023540: Snap Kover, Model 01-2020; Snap Kaps, Model 03-KP09 (2003), 1 descendant of its own
- K041501: Guangzhou Fortunique Drapes, Bags and Covers (2004), 0 descendants of its own

## Recalls of this device
- Jun 18, 2004 · Not classified · Z-1036-04: The product may come apart when excessive force is applied to the coupler.

Source page: https://510kreport.com/device/K850959
Methodology: https://510kreport.com/methodology