# K191881: KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun

- Pathway: 510(k) (Special)
- Applicant: Kbl GmbH
- Decided: Oct 28, 2019 after 105 days
- Product code: LEJ (Booth, Sun Tan)
- Device class: 2
- Regulation: 21 CFR 878.4635
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K151962 (2016). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151962: KBL Sunlamp Products (= Device Bundling name), Kbl AG (2016) Summary page 5.

## Indications for use
KBL Sunlamp Hybrid Products are over-the-counter tanning devices emitting ultraviolet light in the UVB and UVA region of the spectrum intended for tanning of the human skin of an adult person.

Source page: https://510kreport.com/device/K191881
Methodology: https://510kreport.com/methodology