Sonotech, Inc.
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042619 | ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRASOUND IMAGING COUPLANT | MUI | 2004-11-05 | View |
| 510(k) | K033178 | ULTRABIO | MUI | 2004-08-04 | View |
| 510(k) | K031222 | SCANLUBE | MUI | 2003-07-23 | View |
| 510(k) | K031894 | SCANTEC PAD | MUI | 2003-07-18 | View |
| 510(k) | K013701 | ENDO-GLIDE | GCJ | 2002-02-04 | View |
| 510(k) | K013170 | SCANTAC MEMBRANE OR SCANTAC STRIP | ITX | 2001-11-13 | View |
| 510(k) | K984562 | VIVOSONIC | ITX | 1999-06-08 | View |
| 510(k) | K983691 | SCANFLEX SOLID COUPLANT MEMBRANE | ITX | 1999-05-05 | View |
| 510(k) | K983985 | HYBRISONIC SHEATH | ITX | 1999-02-25 | View |
| 510(k) | K981028 | ULTRA IMAGE AND ULTRA SCAN | ITX | 1998-08-21 | View |
| 510(k) | K964658 | OASIS | ITX | 1997-02-14 | View |
| 510(k) | K962093 | ULTRAMIX | ITX | 1996-12-23 | View |
| 510(k) | K961692 | SONOSCAN | ITX | 1996-08-22 | View |
| 510(k) | K953468 | SONOGEL | IYO | 1995-10-17 | View |
No matching devices.
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