FDA 510(k) Applications Submitted by DAVID W MULLIS, JR
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060030 | 01/04/2006 | THE DOUBLE GLOVE | BIOBARRIER, INC. |
| K052637 | 09/26/2005 | THEROX INFUSION CATHETER, MODEL INCA-1 | THEROX, INC. |
| K012881 | 08/28/2001 | C3 ANTERIOR CERVICAL PLATE SYSTEM | SPINE VISION, INC |
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