Crystal Diagnostics, 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) | K910240 | CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST | CHH | 1991-02-26 | View |
| 510(k) | K903126 | CHOLESTAT(TM) WHOLE BLOOD CHOLESTEROL TEST | CHH | 1990-12-26 | View |
No matching devices.
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