FDA 510(k) Applications Submitted by Actuated Medical, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121571 | 05/29/2012 | TUBECLEAR | ACTUATED MEDICAL, INC |
| K220890 | 03/28/2022 | IO Needle Safety Sheath | Actuated Medical, Inc |
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