510(k) K232957

Device
Sterile and Non-Sterile Ultrasound Gels
Applicant
Jianerkang Medical Co., Ltd.
510(k) number
K232957
Product code
MUI
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-15
Date received
2023-09-21
Regulation
892.1570
Classification name
Media, Coupling, Ultrasound
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Zhang Zhigang
Address
#1,Jianerkang Rd., Zhixi Town Industrial Zone Jintan District Changzhou CN 213251 213251

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00197344130279MEDLINEMEDLINE INDUSTRIES, INC.2026-01-23

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