Vistech Consultants, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K882634 | VISUAL CONTRAST SENSITI., POTENTIAL ACUITY&GLARE | HOX | 1988-07-15 | View |
| 510(k) | K881059 | MCT 8000 (MULTI-VISION CONTRAST TESTER) | HOX | 1988-04-04 | View |
| 510(k) | K881021 | VCTS 700S SYSTEM | HOX | 1988-04-01 | View |
| 510(k) | K881022 | VCTS MARKETING PROGRAM SYSTEM | HOX | 1988-04-01 | View |
| 510(k) | K881023 | VCTS 6500 SYSTEM | HOX | 1988-04-01 | View |
| 510(k) | K853481 | VISTECH VCTS GLARE TESTER | HOX | 1985-10-29 | View |
| 510(k) | K840255 | VISTECH VCTS 6000 | HOX | 1984-04-13 | View |
No matching devices.
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