FDA 510(k) Applications Submitted by Stefani Vinkemeier
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K213510 | 11/02/2021 | IMMULITE/IMMULITE 1000 OM-MA, IMMULITE 2000 OM-MA | Siemens Healthcare Diagnostics Products Ltd |
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