Protek Medical Products, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K973958 | GENERAL PURPOSE ATL NEEDLE GUIDE KIT | ITX | 1998-01-22 | View |
| 510(k) | K973622 | TRANSDUCER POSITIONER | ITX | 1997-11-26 | View |
| 510(k) | K970889 | ULTRASOUND TRANSDUCER DRAPE | KKX | 1997-10-20 | View |
| 510(k) | K970893 | ULTRASOUND TRANSDUCER DRAPE | FYA | 1997-10-20 | View |
| 510(k) | K973362 | NEEDLE GUIDE/GRID | ITX | 1997-10-01 | View |
| 510(k) | K970885 | ULTRASOUND SYSTEMS DRAPE | MMP | 1997-09-22 | View |
| 510(k) | K970891 | DRAPE, SURGICAL-LATEX | KKX | 1997-08-22 | View |
| 510(k) | K971722 | TRANS VAGINAL NEEDLE GUIDE | ITX | 1997-07-10 | View |
| 510(k) | K971115 | GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE | ITX | 1997-06-13 | View |
No matching devices.
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