FDA 510(k) Applications Submitted by BIOVISION AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K042083 | 08/03/2004 | MODIFICATION TO VISITOME 20-10 MICROKERATOME | BIOVISION AG |
| K014000 | 12/04/2001 | VISTITOME 20-10 MICROKERATOME | BIOVISION AG |
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