What is FDA product code QIH?

To provide automated radiological image processing and analysis tools. Software implementing artificial intelligence including nonadaptive machine learning algorithms trained with clinical and/or artificial data. In these devices, the algorithm training data typically impacts device performance. Adaptive AI algorithms are not within scope of this product code.

Radiology › Image Processing and StorageAutomated Radiological Image Processing Software

Preview

Name: Preview
Brand: Preview

The Preview Shoulder, a 3D total shoulder arthroplasty (TSA) surgical planning software, is a standalone software application which assists the surgeon in planning reverse and anatomic…

Registry build 21.09.26

The Preview Shoulder, a 3D total shoulder arthroplasty (TSA) surgical planning software, is a standalone software application which assists the surgeon in planning reverse and anatomic shoulder arthroplasty. Preview Shoulder includes 3D digital representations of implants for placement in images used for surgical planning. Preview Shoulder is a secure software application used by qualified or trained surgeons and is accessed by authorized users. The primary function of Preview Shoulder is to receive and process DICOM CT image(s) of patients. Preview Shoulder can be used to place an implant in the original CT image and place an implant in the 3D model of reconstructed bone. The Preview Shoulder allow the user to perform surgical planning and generate an output surgical report. Preview Shoulder does not provide a diagnosis or surgical recommendation. The surgeon is responsible for selecting and placing the implant model for pre-surgical planning purposes.

8manufacturers in China registered for this device type

1catalogue number

2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (4), Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code QIH
Manufacturer	City	Province	Registered as	Device types
Philips Ultrasound (Shanghai) Co., Ltd.	Shanghai	Shanghai	Contract manufacturer	5
GE Medical Systems (China) Co., Ltd.	Wuxi	Jiangsu	Contract manufacturer	57
GE Hangwei Medical Systems Co., Ltd.	Beijing	Beijing	Specification developer	22
GE Healthcare (China) Co., Ltd.	Beijing	Beijing	Specification developer	22
Shanghai United Imaging Healthcare Co., Ltd.	Shanghai	Shanghai	Manufacturer	12
Beijing Infervision Healthcare Medical Technology Co., Ltd.	Beijing	Beijing	Complaint-file establishment	4
Wuhan United Imaging Healthcare Co., Ltd.	Wuhan	Hubei	Manufacturer	4
Keya Medical Technology Co., Ltd.	Beijing	Beijing	Manufacturer	2

Record

Regulatory record for Preview
Listed by	Genesis Software Innovations, United States
FDA product code	QIH
Device type	Automated Radiological Image Processing Software
Device class	Class 2
Regulation	21 CFR 892.2050
Establishment	Manufacturer
510(k)	K210556
Record published	2022-09-27

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Single use	Yes
Prescription	Prescription only
Label carries	lot or batch number

Catalogue Numbers

Catalogue numbers for Preview
Catalogue number	Size	Status
1.29.1		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Imbio RV/LV	Imbio, LLC	5
VEA Align	EOS imaging	4
Qlab Advanced Quantification Software	Philips Ultrasound LLC	3
uOmnispace	Shanghai United Imaging Healthcare Co., Ltd.	3
Scenium	Siemens Medical Solutions USA, Inc.	3
syngo.MI General	Siemens Medical Solutions USA, Inc.	3
Neosoma Dashboard	Neosoma, Inc.	3
BriefCase-Quantification	Aidoc Medical Ltd.	3
OrthoNext™ Platform System Software	Orthofix SRL	3
MI View&GO	Siemens Medical Solutions USA, Inc.	3
FEops	Feops NV	3
AI-Rad Companion Brain MR	Siemens Healthcare Limited	3

Showing 12 of 147. All products under Automated Radiological Image Processing Software

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K240172	2024-04-04
K210556	2021-04-21

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.