Sonotech, Inc.
Sonotech, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2004.
Top product codes for Sonotech, Inc.
Recent clearances by Sonotech, Inc.
- K042619 — ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT
- K033178 — ULTRABIO
- K031222 — SCANLUBE
- K031894 — SCANTEC PAD
- K013701 — ENDO-GLIDE
- K013170 — SCANTAC MEMBRANE OR SCANTAC STRIP
- K984562 — VIVOSONIC
- K983691 — SCANFLEX SOLID COUPLANT MEMBRANE
- K983985 — HYBRISONIC SHEATH
- K981028 — ULTRA IMAGE AND ULTRA SCAN
- K964658 — OASIS
- K962093 — ULTRAMIX
- K961692 — SONOSCAN
- K953468 — SONOGEL
Data sourced from openFDA. This site is unofficial and independent of the FDA.