FDA 510(k) Applications Submitted by MD Diagnostics Limited
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190022 | 01/04/2019 | SafeBreath Filter Mouthpiece | MD Diagnostics Limited |
| K171129 | 04/17/2017 | CO Check Pro, CO Screen | MD Diagnostics Limited |
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