# K771298: 6 L.L. System

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba Medical Systems
- Decided: Aug 3, 1977 after 55 days
- Product code: JAA (System, X-Ray, Fluoroscopic, Image-Intensified)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K993038: Toshiba RTP9211J-G11, J-Advanced Image Intensifier (I.I.) (1999), 1 descendant of its own
- K041027: Digital Radiography System with Flat Panel Detector, Model DFP8000D (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K771298
Methodology: https://510kreport.com/methodology