# K932483: Sundash

- Pathway: 510(k) (Traditional)
- Applicant: Sun Ind., Inc.
- Decided: Feb 22, 1994 after 274 days
- Product code: LEJ (Booth, Sun Tan)
- Device class: 2
- Regulation: 21 CFR 878.4635
- 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Jul 25, 2014 · Class II · Z-2635-2014: The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).

Source page: https://510kreport.com/device/K932483
Methodology: https://510kreport.com/methodology