In Vitro Technologies, 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) | K914685 | 866.5750 RADIOALLERGOSORBENT IMMUNLOGICAL TEST SYS | DHB | 1992-09-14 | View |
| 510(k) | K904661 | IVT RAST TRACER | DHB | 1990-11-29 | View |
| 510(k) | K875329 | IVT CENTRAL ALLERGY SCREEN | DHB | 1988-04-07 | View |
| 510(k) | K875328 | IVT WESTERN ALLERGY SCREEN | DHB | 1988-03-23 | View |
| 510(k) | K874168 | IVT SOUTHEAST ALLERGY SCREEN | DHB | 1988-01-11 | View |
| 510(k) | K874169 | IVT NORTHEAST ALLERGY SCREEN | DHB | 1988-01-11 | View |
| 510(k) | K870625 | IVT SOUTHWEST ALLERGY SCREEN | DHB | 1987-05-01 | View |
No matching devices.
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