FDA 510(k) Applications Submitted by ALAN BUNTING
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970143 | 01/15/1997 | C4 | CLINICON CORP. |
| K040121 | 01/20/2004 | DERMAWAVE 5000 COMBI MAX SYSTEM | DERMAWAVE, LLC |
| K962242 | 06/11/1996 | SURESCAN | CLINICON CORP. |
| K964831 | 12/02/1996 | SURESCAN | CLINICON CORP. |
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