Sense Technology, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K973914 | SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR | LXM | 1998-06-30 | View |
| 510(k) | K940085 | FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01 | LXM | 1994-12-07 | View |
No matching devices.
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