FDA 510(k) Applications Submitted by Teresa Carrow
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220272 | 01/31/2022 | cobas pulse blood glucose monitoring system | Roche Diagnostics |
| K200811 | 03/27/2020 | cobas u 701 microscopy analyzer | Roche Diagnostics |
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