# K992794: Stingray DR, Model 1

- Pathway: 510(k) (Traditional)
- Applicant: Infimed, Inc.
- Decided: Nov 9, 1999 after 82 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K803130 (1981). 12 ancestors in all.
103 later devices descend from it; 4 cite it directly.
0 of 116 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982795: Philips Bucky Vision, Philips Medical Systems, Inc. (1998) Summary page 2.
- K983732: Thorax FD and Multix FD, Siemens Medical Solutions USA, Inc. (1999) Summary page 2.
- K981556: Canon X-Ray Digital Camera Cxdi-11, Canon USA, Inc. (1998) Summary page 2.
- K982196: Digital Radiographic Imaging System, GE Medical Systems (1998) Summary page 2.

## Most influential descendants
- K024147: Paxscan 4030 Medical Digital Imaging System (2003), 78 descendants of its own
- K092669: DX-D Imaging Package (2009), 34 descendants of its own
- K120020: Vivix-S (2012), 30 descendants of its own
- K122865: Vivix-S Wireless (2013), 28 descendants of its own
- K122736: DX-D Imaging Package (2013), 25 descendants of its own

## Indications for use
The Stingray Solid State X-ray Imaging Device is intended for use in general radiographic examinations and applications wherever conventional screen-film systems may be used (excluding fluoroscopy, angiography, and mammography).

Source page: https://510kreport.com/device/K992794
Methodology: https://510kreport.com/methodology