J-Tech, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K954737 | SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICE | HCC | 1996-07-03 | View |
| 510(k) | K954647 | INCLINOMETER | KQX | 1995-10-30 | View |
| 510(k) | K945630 | LARGE MUSCLE STRENGTH GAUGE | KQX | 1995-05-10 | View |
| 510(k) | K913587 | JTECH 50 SERIES CUTTING LOOP | FJL | 1991-10-23 | View |
| 510(k) | K912526 | GS-220 HAND IMPAIRMENT EVALUATION SYSTEM | LBB | 1991-09-05 | View |
No matching devices.
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