FDA 510(k) Applications Submitted by INSIGHT TECHNOLOGIES INSTRUMENTS, LLC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K974243 | 11/12/1997 | KERATOME SYSTEM | INSIGHT TECHNOLOGIES INSTRUMENTS, LLC. |
| K984537 | 12/21/1998 | KERATOME SYSTEM, MODEL K3000 | INSIGHT TECHNOLOGIES INSTRUMENTS, LLC. |
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