FDA 510(k) Applications Submitted by MIKE KYLE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K981304 | 04/10/1998 | NITRILON CORRECT-TOUCH | CT INTL. |
| K981333 | 04/13/1998 | NITRILON CORRECT-TOUCH | BIOPRO (M) SDN BHD |
| K984512 | 12/18/1998 | NITRILON CORRECT-TOUCH | CT INTL. |
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