FDA 510(k) Applications Submitted by JAYESH PATEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071610 | 06/13/2007 | MEDIAID PULSE OXIMETER M30 AND M34 | MEDIAID INC. |
| K071642 | 06/18/2007 | MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER | MEDIAID INC. |
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