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Ultrasound Imaging System For Acquiring Images At Home By Lay Users

Page Type
Product Code
Definition
An ultrasound imaging system for acquiring images at home by lay users is a prescription home use device that may consist of hardware and/or software intended for acquiring ultrasound images for interpretation by a qualified health care professional (e.g., fetal images for determination of fetal heart rate). The device provides guidance to lay users to aid image acquisition.
Physical State
Hardware and/or software for acquiring, processing and displaying ultrasound images
Technical Method
The ultrasound images are acquired in home environment by the lay users using guidance provided by the device software or under direct supervision of a qualified healthcare professional.
Target Area
Human body
Regulation Medical Specialty
Radiology
Review Panel
Radiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
892.1590
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SGJ is linked to regulation 21CFR892.1590, which does not seem to exist yet. It may be pending at the moment.

Ultrasound Imaging System For Acquiring Images At Home By Lay Users

Page Type
Product Code
Definition
An ultrasound imaging system for acquiring images at home by lay users is a prescription home use device that may consist of hardware and/or software intended for acquiring ultrasound images for interpretation by a qualified health care professional (e.g., fetal images for determination of fetal heart rate). The device provides guidance to lay users to aid image acquisition.
Physical State
Hardware and/or software for acquiring, processing and displaying ultrasound images
Technical Method
The ultrasound images are acquired in home environment by the lay users using guidance provided by the device software or under direct supervision of a qualified healthcare professional.
Target Area
Human body
Regulation Medical Specialty
Radiology
Review Panel
Radiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
892.1590
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SGJ is linked to regulation 21CFR892.1590, which does not seem to exist yet. It may be pending at the moment.