FDA 510(k) Applications Submitted by OXYPULSE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100815 | 03/23/2010 | OXIBLUE FINGERTIP PULSE OXIMETER MODEL MD300C318, OXIPRO FINGERTIP PULSE OXIMETER MODEL MD300C316 | OXYPULSE |
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