FDA 510(k) Applications Submitted by CHRIS HORACEK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070964 | 04/05/2007 | KLEENSPEC SINGLE USE VAGINAL SPECULUM AND 790 SERIES CORDLESS ILLUMINATION SYSTEM | WELCH ALLYN, INC. |
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