Clk Intl., 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) | K974371 | CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE | LYY | 1998-04-21 | View |
| 510(k) | K974301 | CLK INT'L. SANITARY LATEX PROBE COVER, CLK ULTRASOUND PROBE COVER | ITX | 1998-02-06 | View |
No matching devices.
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