# K041621: Liteport LP100 Surgical Illuminator

- Pathway: 510(k) (Traditional)
- Applicant: Medical Vision Industries, Inc.
- Decided: Sep 13, 2004 after 89 days
- Product code: FTF (Illuminator, Non-Remote)
- Device class: 2
- Regulation: 21 CFR 878.4580
- 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 K840371 (1984). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K840371: Flexible Illuminator 5, Suncoast Medical Manufacturers, Inc. (1984) Summary page 2.
- K840372: Flexible Illuminator 15, Suncoast Medical Manufacturers, Inc. (1984) Summary page 2.
- K840373: Flexible Illuminator 10, Suncoast Medical Manufacturers, Inc. (1984) Summary page 2.

## Most influential descendants
- K071180: Scintillant Surgical Light, Model 2644-01-0001 (2007), 1 descendant of its own
- K133425: Scintillant Dual Bent Tip Surgical Light, Scintillant Dual Straight Tip Surgical Light (2013), 0 descendants of its own

## Indications for use
The LitePort@ LP100 Surgical Illuminator provides supplemental illumination in surgical procedures in the thoracic and abdominal cavities.

Source page: https://510kreport.com/device/K041621
Methodology: https://510kreport.com/methodology