ClearanceBrief
Company ยท US

Sonotech, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2004. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ITXTransducer, Ultrasonic, Diagnostic8
MUIMedia, Coupling, Ultrasound4
GCJLaparoscope, General & Plastic Surgery1
IYOSystem, Imaging, Pulsed Echo, Ultrasonic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 5, 2004K042619ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT
Sonotech, Inc.
MUI
Aug 4, 2004K033178ULTRABIO
Sonotech, Inc.
MUI
Jul 23, 2003K031222SCANLUBE
Sonotech, Inc.
MUI
Jul 18, 2003K031894SCANTEC PAD
Sonotech, Inc.
MUI
Feb 4, 2002K013701ENDO-GLIDE
Sonotech, Inc.
GCJ
Nov 13, 2001K013170SCANTAC MEMBRANE OR SCANTAC STRIP
Sonotech, Inc.
ITX
Jun 8, 1999K984562VIVOSONIC
Sonotech, Inc.
ITX
May 5, 1999K983691SCANFLEX SOLID COUPLANT MEMBRANE
Sonotech, Inc.
ITX
Feb 25, 1999K983985HYBRISONIC SHEATH
Sonotech, Inc.
ITX
Aug 21, 1998K981028ULTRA IMAGE AND ULTRA SCAN
Sonotech, Inc.
ITX
Feb 14, 1997K964658OASIS
Sonotech, Inc.
ITX
Dec 23, 1996K962093ULTRAMIX
Sonotech, Inc.
ITX
Aug 22, 1996K961692SONOSCAN
Sonotech, Inc.
ITX
Oct 17, 1995K953468SONOGEL
Sonotech, Inc.
IYO

Latest recalls

DateFirm and productCodeLinked 510(k)
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