FDA 510(k) Applications Submitted by CLK INTL., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K974301 | 11/17/1997 | CLK INT'L. SANITARY LATEX PROBE COVER, CLK ULTRASOUND PROBE COVER | CLK INTL., INC. |
| K974371 | 11/20/1997 | CLK INT'L POWDER FREE LATEX EXAMINATION GLOVE | CLK INTL., INC. |
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