# K883779: Wallaby (TM) Blanket

- Pathway: 510(k) (Traditional)
- Applicant: Fiberoptic Medical Products, Inc.
- Decided: Nov 14, 1988 after 69 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.
18 later devices descend from it; 1 cites it directly.
0 of 19 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
- K991627: Wallaby 3 Phototherapy System, Model 3600 (1999), 17 descendants of its own
- K070180: Wallaby 4 (2007), 12 descendants of its own
- K072035: Resolve Uvb Phototherapy System (2007), 6 descendants of its own
- K170489: Skylit Phototherapy System (2017), 5 descendants of its own
- K173436: Luma Light System (2018), 3 descendants of its own

Source page: https://510kreport.com/device/K883779
Methodology: https://510kreport.com/methodology