FDA 510(k) Applications Submitted by David Bostwick
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K242228 | 07/30/2024 | Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01) | Triopsy Medical, Inc. |
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