Equal 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) | K981800 | SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 | HIH | 1998-07-06 | View |
| 510(k) | K961179 | SENTINEL LIPASE LIQUID MODEL 17.401B | CHI | 1996-07-19 | View |
No matching devices.
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