FDA 510(k) Applications Submitted by MEHL/BIOPHILE INTL., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971814 | 05/15/1997 | IMPROVEMENTS TO THE MEHL RUBY LASER | MEHL/BIOPHILE INTL., INC. |
| K980753 | 02/18/1998 | CHROMOSCAN SCANNING SYSTEM | MEHL/BIOPHILE INTL., INC. |
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