FDA 510(k) Applications Submitted by DORIAN SWARTZ
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000639 | 02/25/2000 | VISIONARY 2000 | BURTON MEDICAL PRODUCTS CORP. |
| K023004 | 09/09/2002 | LFRE INDIRECT LARYNGOSCOPE | ASTRALITE CORP. |
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