Khi, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K830404 | RAD VALVE | BTL | 1983-03-17 | View |
| 510(k) | K830399 | COUPLING/VALVE | BTC | 1983-03-10 | View |
| 510(k) | K811858 | KHI CPRAM BREATHING CIRCUIT | CAI | 1981-07-16 | View |
| 510(k) | K800456 | EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR. | BTL | 1980-03-18 | View |
No matching devices.
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