Medical Device Manufacturer · US , Bellingham , WA

Sonotech, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1995

Recent clearances: VIVOSONIC, SCANFLEX SOLID COUPLANT MEMBRANE, HYBRISONIC SHEATH

Total

Cleared

Denied

Sonotech, Inc. has 14 FDA 510(k) cleared radiology devices. Based in Bellingham, US.

Historical record: 14 cleared submissions from 1995 to 2004.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Sonotech, Inc. is one of 7894 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sonotech, Inc.

14 devices

1-12 of 14

Cleared Nov 05, 2004

ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING...

General & Plastic Surgery · 88d

Cleared Nov 13, 2001

SCANTAC MEMBRANE OR SCANTAC STRIP

SCANFLEX SOLID COUPLANT MEMBRANE

ULTRA IMAGE AND ULTRA SCAN

Sonotech, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sonotech, Inc.

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