FDA 510(k) Applications Submitted by INTEL CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101178 | 04/27/2010 | MODIFICATION TO INTEL HEALTH GUIDE PHS6000 | INTEL CORP. |
| K080798 | 03/20/2008 | INTEL HEALTH GUIDE, MODEL: PHS6000 | INTEL CORP. |
| K083115 | 10/21/2008 | MODIFICATION TO INTEL HEALTH GUIDE, MODEL PHS6000 | INTEL CORP. |
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