Uhi Corp.
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) | K843389 | CLINITRON AIR FLUIDIZED SUPPORT J-101UD | INX | 1984-09-05 | View |
| 510(k) | K821835 | BARRIER BURN SHEET | KME | 1982-07-02 | View |
| 510(k) | K813584 | CLINITRON AIR FLUIDIZED SUPPORT SYSTEM | INX | 1982-01-12 | View |
No matching devices.
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