Endotronics, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K875151 | ACUSYST-P/3X | KJH | 1988-01-12 | View |
| 510(k) | K872086 | ACUSYST-JR | KJH | 1987-06-15 | View |
| 510(k) | K864334 | ACUSYST-P (CELL CULTURE EQUIPMENT) | KJH | 1986-11-24 | View |
No matching devices.
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