# K151962: KBL Sunlamp Products (= Device Bundling name)

- Pathway: 510(k) (Traditional)
- Applicant: Kbl AG
- Decided: Sep 15, 2016 after 427 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
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. The FDA summary names its predicate without a number.
- (no number) KBL 6800 alpha: named in the summary without a submission number
- (no number) KBL 7900 alpha: named in the summary without a submission number
- (no number) KBL 4800 alpha: named in the summary without a submission number
- (no number) KBL 5600 alpha: named in the summary without a submission number
- (no number) KBL Tower Space 2000: named in the summary without a submission number
- (no number) KBL Tower Space 3000: named in the summary without a submission number
- (no number) KBL Tower pure Energy 5.0: named in the summary without a submission number

## Most influential descendants
- K191881: KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun (2019), 0 descendants of its own

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

Source page: https://510kreport.com/device/K151962
Methodology: https://510kreport.com/methodology