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Sonotech, Inc.

14 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT (K042619)Sonotech, Inc.2004-11-05
ULTRABIO (K033178)Sonotech, Inc.2004-08-04
SCANLUBE (K031222)Sonotech, Inc.2003-07-23
SCANTEC PAD (K031894)Sonotech, Inc.2003-07-18
ENDO-GLIDE (K013701)Sonotech, Inc.2002-02-04
SCANTAC MEMBRANE OR SCANTAC STRIP (K013170)Sonotech, Inc.2001-11-13
VIVOSONIC (K984562)Sonotech, Inc.1999-06-08
SCANFLEX SOLID COUPLANT MEMBRANE (K983691)Sonotech, Inc.1999-05-05
HYBRISONIC SHEATH (K983985)Sonotech, Inc.1999-02-25
ULTRA IMAGE AND ULTRA SCAN (K981028)Sonotech, Inc.1998-08-21
OASIS (K964658)Sonotech, Inc.1997-02-14
ULTRAMIX (K962093)Sonotech, Inc.1996-12-23
SONOSCAN (K961692)Sonotech, Inc.1996-08-22
SONOGEL (K953468)Sonotech, Inc.1995-10-17

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Every clearance here is in the API, with alerts when new ones post.