# K101833: Infistitch for I5 Digital X-Ray Imaging System, Model I5

- Pathway: 510(k) (Special)
- Applicant: Infimed, Inc.
- Decided: Jul 23, 2010 after 22 days
- Product code: OWB (Interventional Fluoroscopic X-Ray System)
- 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
Longest line of descent: 5 generations back to K803130 (1981). 17 ancestors in all.
1 later device descends 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)
- K093066: I5 Digital X-Ray Imaging System, Model I5, Infimed, Inc. (2010) Summary page 1.

## Most influential descendants
- K111344: I5 Digital X-Ray Imaging System (with Flaatz 560) (2011), 0 descendants of its own

## Indications for use
The InfiMed i*™ Digital X-ray Imaging System is a high resolution digital imaging System intended to replace conventional film techniques, or existing digital systems, in miultipurpose or dedicated applications specified below. The i*™ Digital X-ray Imaging System enables an operator to acquire, display, process, export images to portable media, send images over a network for long term storage and distribute hardcopy images with a laser printer. Image processing algorithms enable the operator to bring out diagnostic details difficult to see using conventional imaging techniques. Images can be stored locally for temporary storage. The i*™ Digital X-ray Imaging System has the ability to interface with a variety of image receptors from CCD cameras to commercially available flat panel detectors. The major system components include an image receptor, computer, monitor and imaging software. For the DR application, the InfiMed i*™ Digital X-ray Imaging System is intended for use in general radiographic examinations and applications (excluding fluoroscopy, angiography, and mammography). For the RF/DSA application, the InfiMed i*™ Digital X-ray Imaging System is intended for use where general fluoroscopy, interventional fluoroscopy or angiography imaging procedures are performed.

Source page: https://510kreport.com/device/K101833
Methodology: https://510kreport.com/methodology