FDA 510(k) Applications Submitted by Steve Adler
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K200313 | 02/06/2020 | VIVO | Catheter Precision, Inc. |
| K183195 | 11/19/2018 | VIVO | Catheter Precision, Inc. |
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