FDA 510(k) Applications Submitted by THEODORE A BOUTACOFF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960522 | 02/06/1996 | DIOPEXY PROBE | IRIDERM DIV. |
| K960971 | 03/11/1996 | OCULIGHT GL | IRIDERM DIV. |
| K964074 | 10/11/1996 | DIOLITE 532 | IRIDERM DIV. |
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