FDA 510(k) Applications Submitted by AFRAME DIGITAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090138 | 01/21/2009 | MOBILECARE MONITOR, MODEL 2100 | AFRAME DIGITAL, INC. |
| K122333 | 08/02/2012 | MOBILECARE MONITOR | AFRAME DIGITAL, INC. |
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