# K090192: Bili Blue F20T12/Bby and F40T12/Bby

- Pathway: 510(k) (Traditional)
- Applicant: Interlectric Corp.
- Decided: Apr 24, 2009 after 87 days
- Product code: LBI (Unit, Neonatal Phototherapy)
- Device class: 2
- Regulation: 21 CFR 880.5700
- Recalls of this device: none
- 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. The FDA summary names its predicate without a number.
- (no number) F40 and F20; Philips Special Blue; Philips Lighting Co., Division of Philips Electronics: named in the summary without a submission number

## Indications for use
Interlectric Bili Blue F20T12/BBY and F40TI2/BBY lamps are used in the treatment of Hyperbilimbinemia in newborn infants. The lamps are placed in commercially available luminaries that will concentrate the blue light energy.

Source page: https://510kreport.com/device/K090192
Methodology: https://510kreport.com/methodology