FDA 510(k) Applications Submitted by BIOFORM MEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070090 | 01/10/2007 | RADIESSE LARYNGEAL IMPLANT | BIOFORM MEDICAL, INC. |
| K060815 | 03/27/2006 | JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT | BIOFORM MEDICAL, INC. |
| K081729 | 06/18/2008 | MODIFICATION TO GFX NERVE ABLATION SYSTEM | BIOFORM MEDICAL, INC. |
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