Laurie Ann Kaiser, Ph.D.
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) | K860552 | PERITONE DISPOSAL SHEATH - RUBBER AND VINYL | HIR | 1986-04-17 | View |
| 510(k) | K800191 | PERITONE | HIR | 1980-04-16 | View |
No matching devices.
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