510(k) K031894

Device
SCANTEC PAD
Applicant
SONOTECH, INC.
510(k) number
K031894
Product code
MUI  
Decision
Substantially Equivalent (SESE)
Decision date
2003-07-18
Date received
2003-06-19
Regulation
892.1570
Classification name
Media, Coupling, Ultrasound
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Special
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
MARGARET J LARSON
Address
774 Marine Dr. Bellingham WA US 98225 98225

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code MUI  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252337EdgeFlow Gel PadEdgecare, Inc.2026-04-24
K242167Sterile and Non-Sterile Ultrasonic Coupling AgentAnhui Deepblue Medical Technology Co., Ltd.2024-09-19
K241789Non-Sterile Ultrasound Transmission GelsHony Medical Co., Ltd.2024-07-24
K221999Ultrasound Transmission GelsHony Medical Co., Ltd.2022-08-30
K211691Ultrast GelUltrast, Inc.2021-12-22
K190591Safergel Sterile Ultrasound GelSafersonic Us, Inc.2019-10-04
K181363EcoVue Sterile and Non-Sterile Ultrasound GelsH R Pharmaceuticals, Inc.2018-06-13
K163026Ultra/Phonic Scanning GelPharmaceutical Innovations, Inc.2018-01-09
K163027Ultra/Phonic Free Conductivity GelPharmaceutical Innovations, Inc.2018-01-09
K163023Other-Sonic Transmission GelPharmaceutical Innovations, Inc.2018-01-08
K163024Ultra/Phonic Conductivity GelPharmaceutical Innovations, Inc.2018-01-08
K163050Advance Medical Designs, Inc. Sterile Ultrasound GelAdvance Medical Designs, Inc.2017-10-25
K151070Sonishield 100 Antimicrobial Ultrasound GelQuotient Medical2016-01-13
K130581KONIX STERILE GELTurkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa2014-06-18
K131905SOLID GEL PADBluemtech2013-07-18

Legacy Summary#

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FDA Review#

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